| Diseases |
Alias |
|
| Meningioma, Familial |
|
Meningioma
|
Familial Meningioma
|
|
Meningioma, Familial, Susceptibility To
|
Meningeal Neoplasm
|
|
Meningeal Neoplasms
|
Meningiomas
|
|
Meningioma, Nf2-Related, Somatic
|
Meningioma, Sis-Related
|
|
Meningothelial Cell Tumor
|
Neoplasm Of The Meninges
|
|
Primary Meningeal Tumor
|
Familial Multiple Meningioma
|
|
MNGMA
|
Meningioma, Benign, No Icd-O Subtype
|
|
Intracranial Meningioma
|
Meningothelial Cell Neoplasm
|
|
Supratentorial Meningioma
|
Primary Neoplasm Of Spinal Meninges
|
|
Benign Intracranial Meningioma
|
Benign Meningioma
|
|
Meningeal Tumours
|
Meningeal Sarcoma Of Unspecified Site
|
|
Meningothelial Sarcoma Of Unspecified Site
|
|
|
| Sudden Infant Death Syndrome |
|
SIDS
|
Sudden Infant Death Syndrome, Susceptibility To
|
|
Cot Death
|
Crib Death
|
|
Sudden Death Of Nonspecific Cause In Infancy
|
Sudden Infant Death
|
|
Death, Sudden, Syndrome, Infant
|
|
|
| Gastrointestinal Stromal Tumor |
|
GIST
|
Gastrointestinal Stromal Tumors
|
|
Gastrointestinal Stromal Sarcoma
|
Gastrointestinal Stromal Tumor, Familial
|
|
Gant
|
Gastrointestinal Stromal Tumour
|
|
Stromal Tumor Of Gastrointestinal Tract
|
Stromal Tumour Of Gastrointestinal Tract
|
|
Gastrointestinal Stromal Neoplasm
|
Paraganglioma And Gastric Stromal Sarcoma
|
|
Plexosarcoma
|
|
|
| Microcephaly |
|
Microencephaly
|
Microcephalus
|
|
Microcephalic
|
Nanocephaly
|
|
Congenital Microcephaly
|
Brain Hypoplasia
|
|
Brain Nondevelopment
|
Cephalic Hypoplasia
|
|
Undeveloped Cerebrum
|
Undeveloped Brain
|
|
Micrencephalon
|
Micrencephaly
|
|
|
| Thyroid Sarcoma |
|
Sarcoma Of The Thyroid Gland
|
Thyroid Gland Sarcoma
|
|
|
| Gingival Overgrowth |
|
Gingival Enlargement
|
Gingival Hyperplasia
|
|
Gingival Bulge
|
Gingival Enlargement Nos
|
|
Gingival Hypertrophy
|
Gum Hypertrophy
|
|
Hyperplasia Gum
|
Gingival Thickening
|
|
Hyperplasia Of Gingiva
|
Hypertrophy Of Gingiva
|
|
Hypertrophy Of Mucous Membrane Of Gums
|
|
|
| Peripheral Nervous System Disease |
|
Peripheral Neuropathy
|
Peripheral Nerve Disease
|
|
Peripheral Nerve Disorders
|
Neuropathy, Peripheral
|
|
Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation
|
|
|
| Paraganglioma |
|
Chemodectoma
|
Glomus Body Tumor
|
|
Paragangliomas
|
Carotid Body Paraganglioma
|
|
Extra-Adrenal Paraganglioma
|
|
|
| Persistent Generalized Lymphadenopathy |
|
Pgl
|
Persistant Generalized Lymphadenopathy
|
|
|
| Central Nervous System Hemangioma |
|
Hemangioma Of Cns
|
Hemangioma Of The Central Nervous System
|
|
|
| Rasopathy |
|
Ras/Mitogen-Activated Protein Kinase Syndrome
|
|
|
| Congenital Central Hypoventilation Syndrome |
|
Cchs
|
Haddad Syndrome
|
|
Ondine Curse
|
Ondine Syndrome
|
|
Congenital Central Hypoventilation
|
Congenital Central Alveolar Hypoventilation Syndrome
|
|
Congenital Failure Of Autonomic Control
|
Ondine'S Curse
|
|
Primary Alveolar Hypoventilation
|
Ondine-Hirschsprung Disease
|
|
Central Congenital Hypoventilation Syndrome
|
Congenital Ondine Curse
|
|
Idiopathic Congenital Central Alveolar Hypoventilation
|
Congenital Central Alveolar Hypoventilation-Hirschsprung Disease Syndrome
|
|
Ondine-Hirschsprung Syndrome
|
|
|
| Thyroid Gland Follicular Carcinoma |
|
Follicular Thyroid Carcinoma
|
Follicular Adenocarcinoma
|
|
Follicular Adenocarcinoma, Well Differentiated
|
Follicular Carcinoma
|
|
Thyroid Adenocarcinoma
|
Adenocarcinoma, Follicular
|
|
|
| Intestinal Obstruction |
|
Inspissated Milk Syndrome
|
Milk Curd Syndrome
|
|
|
| Cowden Syndrome 1 |
|
Pten Hamartoma Tumor Syndrome
|
Bannayan-Riley-Ruvalcaba Syndrome
|
|
Lhermitte-Duclos Disease
|
Bannayan-Zonana Syndrome
|
|
Phts
|
Riley-Smith Syndrome
|
|
Bzs
|
Ruvalcaba-Myhre-Smith Syndrome
|
|
Multiple Hamartoma Syndrome
|
Rmss
|
|
Brrs
|
Dysplastic Gangliocytoma Of The Cerebellum
|
|
CWS1
|
Cs
|
|
Cd
|
Mham
|
|
Pten Hamartoma Tumor Syndrome With Granular Cell Tumor
|
Macrocephaly Multiple Lipomas And Hemangiomata
|
|
Bannayan-Ruvalcaba-Riley Syndrome
|
Myhre-Riley-Smith Syndrome
|
|
LDD
|
Cerebelloparenchymal Disorder Vi
|
|
Hamartoma Syndrome, Multiple
|
Bbrs
|
|
Macrocephaly, Pseudopapilledema, And Multiple Hemangiomata
|
Macrocephaly, Multiple Lipomas, And Hemangiomata
|
|
Macrocephaly Pseudopapilledema And Multiple Hemangiomas
|
Ruvalcaba -Myhre-Smith Syndrome
|
|
Ruvalcaba-Myhre Syndrome
|
Cowden Disease
|
|
Macrocephaly Pseudopapilledema And Multiple Hemangiomata
|
Cerebellar Granule Cell Hypertrophy And Megalencephaly
|
|
Cpd6
|
Lhermitte-Duclos Syndrome
|
|
Pten Hamartoma Tumor Syndromes
|
Cowden Syndrome, Type 1
|
|
|
| Pancreatic Cancer |
|
Pancreatic Carcinoma
|
Familial Pancreatic Carcinoma
|
|
Pancreatic Neoplasm
|
Carcinoma Of Pancreas
|
|
Pancreatic Carcinoma, Familial
|
Malignant Neoplasm Of Pancreas
|
|
Pancreatic Acinar Carcinoma
|
Pancreatic Tumor
|
|
Familial Pancreatic Cancer
|
Neoplasm Of The Pancreas
|
|
Pancreatic Carcinoma, Somatic
|
Pancreatic Cancer, Somatic
|
|
Ca Body Of Pancreas
|
Ca Head Of Pancreas
|
|
Ca Tail Of Pancreas
|
Malignant Neoplasm Of Body Of Pancreas
|
|
Malignant Neoplasm Of Head Of Pancreas
|
Malignant Neoplasm Of Tail Of Pancreas
|
|
Pancreas Neoplasm
|
Exocrine Cancer
|
|
Exocrine Pancreas Carcinoma
|
Hereditary Pancreatic Cancer
|
|
Hereditary Pancreatic Carcinoma
|
PNCA
|
|
Cancer Of The Pancreas
|
Pancreatic Cancer, Susceptibility To
|
|
Carcinoma Of Head Of Pancreas
|
Pancreatic Neoplasms
|
|
Pancreatic Tumors
|
Cancer, Pancreatic
|
|
Cancer Of Pancreas
|
Mixed Islet Cell With Exocrine Carcinoma Of Unspecified Site
|
|
|
| Thyroid Carcinoma |
|
Thyroid Cancer
|
Malignant Neoplasm Of Thyroid
|
|
Thyroid Neoplasm
|
|
|
| Parathyroid Gland Disease |
|
Parathyroid Diseases
|
Disease Of Parathyroid Glands
|
|
Parathyroid Disease
|
|
|
| Adrenal Carcinoma |
|
Adrenal Cancer
|
Adrenal Gland Cancer
|
|
Malignant Neoplasm Of Adrenal Gland
|
Adrenal Gland Neoplasms
|
|
Carcinoma Of The Adrenal Gland
|
Adrenal Neoplasm
|
|
Malignant Adrenal Tumor
|
Neoplasm Of Adrenal Gland
|
|
Tumor Of The Adrenal Gland
|
Adrenal Gland Neoplasm
|
|
Adrenocortical Carcinoma
|
Adrenal Gland Malignancy
|
|
Suprarenal Cancer
|
Malignant Neoplasm Of Suprarenal Gland
|
|
Malignant Neoplasm Of Adrenal Gland, Unspecified
|
Malignant Tumour Of Adrenal Gland
|
|
Suprarenal Gland Cancer
|
Primary Malignant Neoplasm Of Adrenal Gland
|
|
|
| Thyroid Tumor |
|
|
| Ovarian Germ Cell Teratoma |
|
Germ Cell Teratoma Of Ovary
|
Ovarian Teratoma
|
|
|
| Papillary Carcinoma |
|
Carcinoma, Papillary
|
Carcinoma Papillary
|
|
|
| Lung Sarcomatoid Carcinoma |
|
Pulmonary Sarcomatoid Carcinoma
|
Sarcomatoid Carcinoma Of The Lung
|
|
|
| Motor Neuron Disease |
|
Anterior Horn Cell Disease
|
Motor Neuron Diseases
|
|
Mnd - [Motor Neurone Disease]
|
Lou Gehrig Disease
|
|
Creeping Palsy
|
Creeping Paralysis
|
|
Bulbar Motor Neuron Disease
|
Bulbar Syndrome
|
|
Anterior Horn Cell Disorder
|
Hereditary Motor Neuron Disease
|
|
|
| Substernal Goiter |
|
Retrosternal Thyroid Goiter
|
Retrosternal Thyroid Goitre
|
|
Substernal Goitre
|
Goiter, Substernal
|
|
|
| Atypical Follicular Adenoma |
|
|
| Multicentric Papillary Thyroid Carcinoma |
|
Multicentric Thyroid Gland Papillary Carcinoma
|
|
|
| Follicular Adenoma |
|
Follicular Adenoma Of The Thyroid Gland
|
Thyroid Follicular Adenoma
|
|
Adenoma Follicular
|
Follicular Thyroid Adenoma
|
|
Thyroid Gland Follicular Adenoma
|
|
|
| Hashimoto Thyroiditis |
|
Autoimmune Thyroiditis
|
Hashimoto Struma
|
|
Hashimoto'S Thyroiditis
|
Chronic Lymphocytic Thyroiditis
|
|
Lymphocytic Thyroiditis
|
Hashimoto Disease
|
|
Ht
|
Hashimoto'S Disease
|
|
Hashimoto'S Syndrome
|
Hypothyroidism, Autoimmune
|
|
Autoimmune Chronic Lymphocytic Thyroiditis
|
Chronic Lymphocytic Thyroiditides
|
|
Hashimoto Syndrome
|
Hashimotos Thyroiditis
|
|
Hashimoto Thyroiditis, Susceptibility To
|
Thyroiditis, Autoimmune
|
|
Lymphomatous Thyroiditis
|
Lymphoid Thyroiditis
|
|
Chronic Lymphadenoid Thyroiditis
|
Autoimmune Lymphocytic Chronic Thyroiditis
|
|
Goitre Lymphomatosa
|
Hashitoxicosis
|
|
Hashimoto Hypothyroidism
|
Lymphadenoid Goitre
|
|
Struma Lymphomatosa
|
Hyperthyroidism With Hashimoto Disease
|
|
Hashimoto Thyrotoxicosis
|
Thyrotoxicosis Due To Hashimoto Thyroiditis
|
|
Struma Lymphomatosis
|
Lymphadenoid Struma
|
|
|
| Cerebral Angioma |
|
Hemangioma Of Cerebrum
|
Cerebral Hemangioma
|
|
|
| American Histoplasmosis |
|
Infection By Histoplasma Capsulatum
|
|
|
| Autonomic Nervous System Benign Neoplasm |
|
|
| Familial Hypocalciuric Hypercalcemia |
|
Familial Benign Hypercalcemia
|
Fbh
|
|
Fbhh
|
Fhh
|
|
Familial Benign Hypocalciuric Hypercalcemia
|
Hypocalciuric Hypercalcemia, Familial, Type 1
|
|
|
| Hyperparathyroidism 2 With Jaw Tumors |
|
Hyperparathyroidism-Jaw Tumor Syndrome
|
Hpt-Jt
|
|
HRPT2
|
Familial Primary Hyperparathyroidism With Multiple Ossifying Jaw Fibromas
|
|
Parathyroid Adenoma With Cystic Changes
|
Hereditary Hyperparathyroidism-Jaw Tumor Syndrome
|
|
Hyperparathyroidism 2
|
Hyperparathyroidism, Familial Primary, With Multiple Ossifying Jaw Fibromas
|
|
Hyperparathyroidism-Jaw Tumor Syndrome, Hereditary
|
Familial Cystic Parathyroid Adenomatosis
|
|
Hyperparathyroidism-Jaw Tumor Syndrome, Type 2
|
Parathyroid Adenomatosis, Familial Cystic
|
|
|
| Multiple Endocrine Neoplasia, Type Iib |
|
Multiple Endocrine Neoplasia Type 2b
|
MEN2B
|
|
Wagenmann-Froboese Syndrome
|
Multiple Endocrine Neoplasia Iib
|
|
Mucosal Neuroma Syndrome
|
Multiple Endocrine Neoplasia, Type 3
|
|
Multiple Endocrine Neoplasia, Type 2b
|
Men Iib
|
|
Neuromata, Mucosal, With Endocrine Tumors
|
Multiple Endocrine Neoplasia, Type Iii, Formerly
|
|
Men3, Formerly
|
Men Type Iib
|
|
Men 2b
|
Multiple Endocrine Neoplasia Type 3
|
|
Multiple Neoplasia 2b
|
Neoplasia, Endocrine, Multiple, Type Iib
|
|
|
| Neuroendocrine Tumor |
|
Neuroendocrine Neoplasm
|
Neuroendocrine Tumors
|
|
Carcinoma, Neuroendocrine
|
|
|
| Hypertelorism |
|
Eyes Wide Apart
|
Eyes Widely Set
|
|
Hypertelorism Of Orbit
|
Ocular Hypertelorism
|
|
Orbital Separation Excessive
|
|
|
| Retinitis Pigmentosa |
|
RP
|
Rod-Cone Dystrophy
|
|
Autosomal Recessive Retinitis Pigmentosa
|
Non-Syndromic Retinitis Pigmentosa
|
|
Pericentral Pigmentary Retinopathy
|
Pigmentary Retinopathy
|
|
Tapetoretinal Degeneration
|
Rcd
|
|
Retinitis Pigmentosa Autosomal Recessive
|
ARRP
|
|
Retinitis Pigmentosa, Autosomal Recessive
|
Retinitis Pigmentosa 1
|
|
|
| Hereditary Breast Ovarian Cancer Syndrome |
|
Hereditary Breast And Ovarian Cancer Syndrome
|
Brca1- And Brca2-Associated Hereditary Breast And Ovarian Cancer
|
|
Breast And/Or Ovarian Cancer
|
Breast And Ovarian Cancer Syndrome
|
|
Hboc Syndrome
|
Hereditary Breast And Ovarian Cancer
|
|
Brca1- Brca2-Associated Hboc
|
|
|
| Cakut |
|
Renal Or Urinary Tract Malformation
|
Congenital Anomalies Of Kidney And Urinary Tract
|
|
Congenital Anomaly Of Kidney And Urinary Tract
|
Congenital Anomalies Of The Kidney And Urinary Tract
|
|
Kidney And Urinary Tract, Anomalies, Congenital
|
Renal Hypodysplasia, Nonsyndromic, 1
|
|
|
| Retinal Degeneration |
|
|
| Sublingual Gland Cancer |
|
Malignant Tumor Of Sublingual Gland
|
Malignant Tumor Of The Sublingual Gland
|
|
|
| Adenocarcinoma |
|
Adenocarcinomas
|
Adenoacanthoma Of Unspecified Site
|
|
Adenocarcinoid Of Unspecified Site
|
Adenocarcinoid Tumour Of Unspecified Site
|
|
Adenocarcinoma And Carcinoid Combined Of Unspecified Site
|
Adenocarcinoma Nos
|
|
|
| Peripheral Nervous System Benign Neoplasm |
|
|
| Parathyroid Carcinoma |
|
Parathyroid Cancer
|
Parathyroid Neoplasms
|
|
Malignant Tumor Of Parathyroid Gland
|
PRTC
|
|
Carcinoma Of Parathyroid Gland
|
Malignant Neoplasm Of Parathyroid Gland
|
|
Parathyroid Gland Adenocarcinoma
|
Parathyroid Gland Cancer
|
|
Parathyroid Neoplasm
|
Parathyroid Gland Carcinoma
|
|
Malignant Neoplasm Of The Parathyroid
|
Neoplasm Of Parathyroid Gland
|
|
Parathyroid Gland Neoplasm
|
Cancer Of The Parathyroid
|
|
Cancer Of The Parathyroid Gland
|
Malignant Neoplasm Of Parathyroid
|
|
Malignant Parathyroid Gland Neoplasm
|
Malignant Parathyroid Gland Tumor
|
|
Malignant Parathyroid Neoplasm
|
Malignant Parathyroid Tumor
|
|
Malignant Tumor Of Parathyroid
|
Parathyroid Adenocarcinoma
|
|
Neoplasm Of The Parathyroid Gland
|
Carcinoma, Parathyroid
|
|
|
| Thyroid Gland Anaplastic Carcinoma |
|
Anaplastic Thyroid Carcinoma
|
Anaplastic Thyroid Cancer
|
|
Thyroid Cancer, Anaplastic
|
Thyroid Carcinoma, Anaplastic
|
|
Thyroid Carcinoma Anaplastic
|
|
|
| Thyroid Gland Disease |
|
Abnormality Of The Thyroid Gland
|
Thyroid Diseases
|
|
|
| Renal Agenesis, Bilateral |
|
|
| Thyroid Gland Medullary Carcinoma |
|
Medullary Thyroid Carcinoma
|
Medullary Carcinoma Of The Thyroid Gland
|
|
Ultimobranchial Thyroid Tumor
|
Ultimobranchial Thyroid Tumour
|
|
Thyroid Cancer, Medullary
|
|
|
| Achalasia |
|
Cardiospasm
|
Achalasia Of Cardia
|
|
Esophageal Achalasia
|
Hypertensive Lower Esophageal Sphincter
|
|
Idiopathic Achalasia
|
Achalasia Cardia
|
|
Idiopathic Achalasia Of Esophagus
|
Primary Achalasia
|
|
Achalasia Of Esophagus
|
Lack Of Reflex Relaxation Of Lower Oesophageal Sphincter
|
|
Aperistalsis Of The Oesophagus
|
Achalasia Of Oesophagus
|
|
Oesophageal Achalasia
|
Achalasia Nos
|
|
Cardia Spasm
|
Cardia Achalasia
|
|
Oesophageal Cardiospasm
|
Oesophagus Achalasia
|
|
Reflex Cardiospasm
|
|
|
| Islet Cell Tumor |
|
Pancreatic Neuroendocrine Tumor
|
Neuroendocrine Tumor Of Pancreas
|
|
Pnet
|
Pancreatic Net
|
|
Well-Differentiated Nen Of Pancreas
|
Well-Differentiated Neuroendocrine Neoplasm Of Pancreas
|
|
Well-Differentiated Pancreatic Nen
|
Well-Differentiated Pancreatic Neuroendocrine Neoplasm
|
|
Endocrine Pancreas Cancer
|
Islet Cell Neoplasm
|
|
Islet Cell Tumour
|
Malignant Pancreatic Endocrine Tumor
|
|
Malignant Pancreatic Endocrine Tumour
|
Malignant Tumor Of Endocrine Pancreas
|
|
Malignant Tumour Of Endocrine Pancreas
|
Pancreatic Endocrine Neoplasm
|
|
Pancreatic Endocrine Tumor
|
Pancreatic Neuroendocrine Neoplasm
|
|
Adenoma, Islet Cell
|
Well Differentiated Pancreatic Endocrine Tumor
|
|
Malignant Neoplasm Of Endocrine Pancreas
|
Pancreatic Endocrine Carcinoma
|
|
|
| Multinodular Goiter |
|
|
| Ovarian Germ Cell Cancer |
|
Ovarian Germ Cell Tumor
|
Malignant Germ Cell Tumor Of Ovary
|
|
Germ Cell Neoplasm Of Ovary
|
Germ Cell Tumor Of Ovary
|
|
Mogct
|
Malignant Ovarian Germ Cell Tumor
|
|
Malignant Ovarian Germ Cell Neoplasm
|
|
|
| Extra-Adrenal Pheochromocytoma |
|
Pheochromocytoma, Extra-Adrenal
|
|
|
| Testicular Spermatocytic Seminoma |
|
|
| Benign Struma Ovarii |
|
|
| Laurence-Moon Syndrome |
|
LNMS
|
Laurence-Moon-Biedl Syndrome
|
|
|
| Multiple Endocrine Neoplasia, Type Iia |
|
Multiple Endocrine Neoplasia Type 2a
|
Sipple Syndrome
|
|
Multiple Endocrine Neoplasia Type 2
|
MEN2A
|
|
Men2
|
Ptc Syndrome
|
|
Multiple Endocrine Neoplasia, Type 2
|
Multiple Endocrine Neoplasia Iia
|
|
Men 2a
|
Multiple Endocrine Neoplasia, Type 2a
|
|
Pheochromocytoma And Amyloid-Producing Medullary Thyroid Carcinoma
|
Multiple Endocrine Neoplasia Ii
|
|
Men2 Syndrome
|
Men-2a Syndrome
|
|
Pheochromocytoma And Amyloid Producing Medullary Thyroid Carcinoma
|
Multiple Neoplasia 2a
|
|
Multiple Neoplasia Type 2
|
|
|
| Neuronal Intestinal Dysplasia, Type B |
|
Neuronal Intestinal Dysplasia Type B
|
Nid B
|
|
|
| Tall Cell Variant Papillary Carcinoma |
|
Tall Cell Variant Thyroid Gland Papillary Carcinoma
|
|
|
| Neuroblastoma |
|
Nb
|
Neuroblastoma, Susceptibility To
|
|
Neuroblastomas
|
Central Neuroblastoma
|
|
|
| Goldberg-Shprintzen Syndrome |
|
Goldberg-Shprintzen Megacolon Syndrome
|
GOSHS
|
|
Megacolon-Microcephaly Syndrome
|
|
|
| Laryngeal Neuroendocrine Tumor |
|
Laryngeal Neuroendocrine Tumour
|
Neuroendocrine Tumor Of Larynx
|
|
Neuroendocrine Tumour Of Larynx
|
Neuroendocrine Neoplasm Of Larynx
|
|
|
| Hypertension, Essential |
|
Essential Hypertension
|
Hypertension
|
|
High Blood Pressure
|
Hypertension, Essential, Susceptibility To
|
|
Hypertensive Disease
|
Primary Hypertension
|
|
EHT
|
Hypertension, Salt-Sensitive Essential, Susceptibility To
|
|
Hyperpiesia
|
Idiopathic Hypertension
|
|
Hypertensive Disorder
|
Hypertension, Essential, Susceptibility To, 3
|
|
Hypertension, Essential 3
|
Hypertension, Essential, Salt-Sensitive
|
|
Hypertension, Essential, Susceptibility To, 6
|
Hypertension, Essential 6
|
|
Hypertension, Salt-Sensitive Essential
|
Hypertension, Susceptibility To
|
|
Hypertension, Essential, Susceptibility To, 4
|
Hypertension, Essential 4
|
|
Hypertension, Essential, Susceptibility To, 2
|
Hypertension, Essential 2
|
|
Hypertension, Essential, Susceptibility To, 1
|
Hypertension, Essential 1
|
|
Hypertension, Essential, Susceptibility To, 5
|
Hypertension, Essential 5
|
|
Htn
|
Vascular Hypertensive Disorder
|
|
Systemic Primary Arterial Hypertension
|
Hbp - [High Blood Pressure]
|
|
Systemic Arterial Hypertensive Disorder
|
Elevated Blood Pressure
|
|
Arterial Hypertension Nos
|
Hypertension Nos
|
|
Benign Hypertension
|
Systemic Arterial Hypertension
|
|
Systemic Hypertension
|
Artery Htn
|
|
Benign Htn
|
Vascular Htn
|
|
Vascular Hypertension
|
Cholesterol Hypertension
|
|
Cholesterol Htn
|
Idiopathic Htn
|
|
Malignant Hypertension
|
Malignant Htn
|
|
Raised Blood Pressure
|
Cardiovascular Hypertension
|
|
Primary Htn - [Hypertension]
|
High Arterial Tension
|
|
High Blood Pressure Disorder
|
Ht - [Hypertension]
|
|
Htn - [Hypertension]
|
Hypertensive Vascular Disease
|
|
Hypertensive Vascular Degeneration
|
|
|
| Thyroid Carcinoma, Familial Medullary |
|
Medullary Thyroid Carcinoma
|
Familial Medullary Thyroid Carcinoma
|
|
MTC
|
Fmtc
|
|
Mtc1
|
Thyroid Cancer, Medullary
|
|
Medullary Thyroid Cancer
|
Thyroid Carcinoma, Medullary
|
|
Familial Mtc
|
Thyroid Carcinoma Medullary
|
|
Carcinoma, Thyroid, Medullary, Familial
|
Medullary Carcinoma Of Thyroid
|
|
Medullary Carcinoma With Amyloid Stroma, Unspecified Site
|
Medullary Carcinoma With Amyloid Stroma Of Thyroid
|
|
|
| Pituitary Adenoma |
|
Pituitary Neoplasms
|
Adenoma Of The Pituitary Gland
|
|
Pituitary Adenomas
|
Adenoma, Pituitary
|
|
Pituitary Gland Adenoma
|
|
|
| Childhood Fibrosarcoma |
|
|
| Skin Lipoma |
|
Lipoma Of Skin
|
Cutaneous Lipoma
|
|
Cutaneous Lipomatous Tumor
|
Lipoma Of Face
|
|
Cutaneous Lipomatous Neoplasm
|
|
|
| Mowat-Wilson Syndrome |
|
MOWS
|
Microcephaly, Mental Retardation, And Distinct Facial Features, With Or Without Hirschsprung Disease
|
|
Hirschsprung Disease-Mental Retardation Syndrome
|
Mowat-Wilson Syndrome Due To Monosomy 2q22
|
|
Hirschsprung Disease Mental Retardation Syndrome
|
Microcephaly, Mental Retardation, And Distinct Facial Featrues, With Or Without Hirschprung Disease
|
|
Hirschsprung Disease - Intellectual Disability Syndrome
|
Hirschsprung Disease Intellectual Disability Syndrome
|
|
Intellectual Disability, Microcephaly, And Distinct Facial Features With Or Without Hirschsprung Disease
|
Mws
|
|
Hirschsprung Disease-Intellectual Disability Syndrome
|
Hirschsprung Disease And Intellectual Disability Due To 2q22 Microdeletion
|
|
Hirschsprung Disease And Intellectual Disability Due To Del(2)(Q22)
|
Hirschsprung Disease And Intellectual Disability Due To Monosomy 2q22
|
|
Mowat-Wilson Syndrome Due To 2q22 Microdeletion
|
Mowat-Wilson Syndrome Due To Del(2)Q(22)
|
|
Mowat-Wilson Syndrome Due To A Zeb2 Point Mutation
|
Hirschsprung Disease And Intellectual Disability Due To A Zeb2 Point Mutation
|
|
|
| Renal Cell Carcinoma, Nonpapillary |
|
Renal Cell Carcinoma
|
RCC
|
|
Nonpapillary Renal Cell Carcinoma
|
Clear Cell Renal Cell Carcinoma
|
|
Hypernephroma
|
Adenocarcinoma Of Kidney
|
|
Renal Carcinoma, Chromophobe, Somatic
|
Clear Cell Carcinoma Of Kidney
|
|
Clear-Cell Metastatic Renal Cell Carcinoma
|
Clear Cell Renal Carcinoma
|
|
Renal Cell Carcinoma, Somatic
|
Conventional Renal Cell Carcinoma
|
|
Conventional Renal Cell Carcinoma
|
Renal Clear Cell Carcinoma
|
|
Ccrcc
|
Hereditary Clear Cell Renal Cell Carcinoma
|
|
Carcinoma, Renal Cell
|
Renal Cell Carcinoma, Clear Cell, Somatic
|
|
Renal Cell Carcinoma, Clear Cell
|
Clear Cell Kidney Carcinoma
|
|
Clear Cell Rcc
|
Cystic-Multilocular Variant
|
|
Clear Cell Renal Cell Adenocarcinoma
|
Hereditary Clear Cell Renal Cell Adenocarcinoma
|
|
Common Renal Cell Carcinoma
|
Crcc
|
|
Renal Cell Carcinoma Non-Papillary
|
Carcinoma Renal Cell
|
|
Renal Cell Cancer
|
Carcinoma, Renal Cell, Nonpapillary
|
|
|
| Primary Hyperparathyroidism |
|
Familial Primary Hyperparathyroidism
|
Hyperparathyroidism, Primary
|
|
Hyperparathyroidism Primary
|
Hypocalciuric Hypercalcemia, Familial, Type 1
|
|
Familial Benign Hypercalcemia
|
Familial Hyperparathyroidism
|
|
Parathyroid Enlargement
|
|
|
| Waardenburg'S Syndrome |
|
Waardenburg Syndrome
|
Van Der Hoeve Halbertsma Waardenburg Gualdi Syndrome
|
|
Van Der Hoeve Halbertsona Waardenburg Syndrome
|
Waardenburg Shah Syndrome
|
|
Waardenburg, Types I And/Or Ii
|
Mende Syndrome
|
|
Waardenburgs Syndrome
|
Waardenburg Syndrome, Type 4a
|
|
|
| Thyroid Lymphoma |
|
|
| Rhabdomyosarcoma |
|
|
| Central Hypoventilation Syndrome, Congenital, 1 |
|
Cchs
|
CCHS1
|
|
Central Hypoventilation Syndrome, Congenital
|
Congenital Failure Of Autonomic Control
|
|
Autonomic Control, Congenital Failure Of
|
Ondine Curse, Congenital
|
|
Central Hypoventilation Syndrome, Congenital, 1, With Or Without Hirschsprung Disease
|
Ondine Curse
|
|
Central Hypoventilation Syndrome, Congenital, 1, With Or Without Hirschsprung
|
Hypoventilation, Central, Syndrome, Congenital, Type 1
|
|
Congenital Central Hypoventilation
|
Sleep Apnea, Central
|
|
Central Alveolar Hypoventilation Syndrome
|
Cchs With Hirschsprung Disease
|
|
Congenital Central Alveolar Hypoventilation Syndrome
|
Sleep-Related Respiratory Failure
|
|
Hypoventilation
|
|
|
| Thyroid Dyshormonogenesis 2a |
|
TDH2A
|
Iodide Peroxidase Deficiency
|
|
Deficiency Of Iodide Peroxidase
|
Thyroid Peroxidase Deficiency
|
|
Genetic Defect In Thyroid Hormonogenesis 2a
|
Thyroid Hormonogenesis, Genetic Defect In, 2a
|
|
Hypothyroidism, Congenital, Due To Dyshormonogenesis, 2a
|
Chdh2a
|
|
Congenital Hypothyroidism Due To Dyshormonogenesis Type 2a
|
Thyroid Hormone Organification Defect 2
|
|
Tiod
|
|
|
| Spitzoid Melanoma |
|
|
| Hemangioma |
|
|
| Renal Hypodysplasia/Aplasia 3 |
|
RHDA3
|
Renal Agenesis, Unilateral
|
|
Unilateral Renal Agenesis
|
|
|
| Neuroma |
|
|
| Tetralogy Of Fallot |
|
TOF
|
Fallot Tetralogy
|
|
Ventricular Septal Defect With Pulmonary Stenosis Or Atresia, Dextraposition Of Aorta, And Hypertrophy Of Right Ventricle
|
Tetrad Of Fallot
|
|
Fallot Tetrad
|
Fallot Disease
|
|
Fallot Complex
|
Subpulmonic Stenosis, Ventricular Septal Defect, Overriding Aorta, And Right Ventricular Hypertrophy
|
|
Interventricular Septal Defect With Dextroposition Of Aorta, Pulmonary Stenosis And Hypertrophy Of Right Ventricle
|
Interventricular Septal Defect, In Tetralogy Of Fallot
|
|
Ventricular Septal Defect With Obstructed Right Ventricular Outflow
|
Tof - [Tetralogy Of Fallot]
|
|
Pulmonary Atresia With Ventricular Septal Defect [Fallot Type]
|
Pulmonary Atresia, Ventricular Septal Defect And Mapcas
|
|
Pulmonary Atresia With Ventricular Septal Defect And Systemic-To-Pulmonary Collateral Arteries [Fallot Type]
|
|
|
| Pheochromocytoma |
|
Pheochromocytoma, Susceptibility To
|
Phaeochromocytoma
|
|
Adrenal Gland Chromaffin Paraganglioma
|
Adrenal Gland Chromaffinoma
|
|
Adrenal Gland Paraganglioma
|
Adrenal Gland Pheochromocytoma
|
|
Chromaffin Paraganglioma Of The Adrenal Gland
|
Intraadrenal Paraganglioma
|
|
PCC
|
Chromaffin Cell Tumor
|
|
Medullary Chromaffinoma
|
Medullary Paraganglioma
|
|
Pheochromoblastoma
|
Pheochromocytomas
|
|
Chromaffin Cell Neoplasm
|
Pheochromocytoma, Malignant
|
|
|
| Medullary Sponge Kidney |
|
Cacchi-Ricci Disease
|
Msk
|
|
Precalicial Canalicular Ectasia
|
Cacchi Ricci Disease
|
|
Cacchi-Ricci Syndrome
|
Cystic Dilatation Of Renal Collecting Tubes
|
|
Precalyceal Canalicular Ectasia
|
Sponge Kidney
|
|
Congenital Cystic Kidney Disease
|
Msk - [Medullary Sponge Kidney]
|
|
Sponge Kidney Nos
|
|
|
| Thyroiditis |
|
Inflammation Of Thyroid
|
Thyroiditis Nos
|
|
|
| Endocrine Organ Benign Neoplasm |
|
|
| Hereditary Paraganglioma-Pheochromocytoma Syndromes |
|
Hereditary Pheochromocytoma-Paraganglioma
|
Hereditary Paraganglioma-Pheochromocytoma
|
|
Familial Pheochromocytoma-Paraganglioma
|
Paragangliomas 2
|
|
Paragangliomas 3
|
Paragangliomas 4
|
|
Sdhx-Related Paraganglioma-Pheochromocytoma
|
Familial Paraganglioma Syndrome
|
|
Familial Paraganglioma-Pheochromocytoma Syndromes
|
Fpgl
|
|
Fpgl/Pheo
|
Paragangliomas 1
|
|
Paraganglioma
|
|
|
| Rare Tumor |
|
|
| Hirschsprung Disease 1 |
|
Hirschsprung Disease
|
Aganglionic Megacolon
|
|
Hscr
|
Congenital Megacolon
|
|
Colonic Aganglionosis
|
Hirschsprung Disease, Susceptibility To, 1
|
|
Hirschsprung Disease, Protection Against
|
Hirschsprung'S Disease
|
|
Congenital Intestinal Aganglionosis
|
HSCR1
|
|
Mgc
|
Pelvirectal Achalasia
|
|
Total Intestinal Aganglionosis
|
Megacolon, Aganglionic
|
|
Macrocolon
|
Hscr 1
|
|
Hirschsprung Disease Type 1
|
Hirschsprung Disease, Type 1
|
|
Congenital Dilatation Of Colon
|
Aganglionosis
|
|
Congenital Aganglionic Megacolon
|
Aganglionosis Of Colon
|
|
Bowel Aganglionosis
|
Colon Aganglionosis
|
|
Hirschsprung Megacolon
|
|
|
| Multiple Endocrine Neoplasia, Type Iv |
|
Multiple Endocrine Neoplasia Type 4
|
MEN4
|
|
Multiple Endocrine Neoplasia 4
|
Neoplasia, Endocrine, Multiple, Type Iv
|
|
|
| Trichothiodystrophy 4, Nonphotosensitive |
|
Amish Brittle Hair Brain Syndrome
|
TTD4
|
|
Trichothiodystrophy, Nonphotosensitive 1
|
Hair-Brain Syndrome
|
|
Bids Syndrome
|
Ttdn1
|
|
Abhs
|
Pollitt Syndrome
|
|
Trichothiodystrophy-Neurocutaneous Syndrome
|
Nonphotosensitive Trichothiodystrophy 4
|
|
Trichorrhexis Nodosa Syndrome
|
Trichothiodystrophy 4, Non-Photosensitive
|
|
Trichothiodystrophy Non-Photosensitive 1
|
|
|
| Endocrine Gland Cancer |
|
Endocrine Neoplasm
|
Malignant Neoplasm Of Endocrine Gland
|
|
Endocrine Gland Neoplasms
|
Endocrine Tumor
|
|
Malignant Endocrine Tumor
|
Malignant Tumour Of Endocrine Gland
|
|
Neoplasm Of Endocrine Gland
|
Neoplasm Of Endocrine System
|
|
Neoplasm Of The Endocrine System
|
Carcinoma Of Endocrine Gland
|
|
|
| Hyperparathyroidism |
|
Hyperparathyroidism And Other Disorders Of Parathyroid Gland
|
Parathyroid Hyperfunction
|
|
Hpth - [Hyperparathyroidism]
|
Parathyroid Gland Hyperfunction
|
|
Parathyroid Glandular Hyperfunction
|
|
|
| Ganglioneuroma |
|
|
| Neurofibromatosis |
|
Neurofibromatoses
|
Acoustic Neurofibromatosis
|
|
Central Neurofibromatosis
|
Peripheral Neurofibromatosis
|
|
Recklinghausen'S Neurofibromatosis
|
Von Reklinghausen Disease
|
|
Neurofibromatosis Type 1
|
|
|
| Nonencapsulated Sclerosing Carcinoma |
|
Nonencapsulated Sclerosing Neoplasm
|
Papillary Carcinoma, Diffuse Sclerosing
|
|
|
| Struma Ovarii |
|
|
| Sensorineural Hearing Loss |
|
Sensory Hearing Loss
|
Sensorineural Hearing Loss Disorder
|
|
Hearing Loss, Sensorineural
|
Central Hearing Loss
|
|
High Frequency Deafness
|
High Frequency Hearing Loss
|
|
High-Frequency Hearing Loss
|
Perceptive Deafness
|
|
Perceptive Hearing Loss
|
Perceptive Hearing Loss Or Deafness
|
|
Sensorineural Deafness
|
Hearing Loss Sensorineural
|
|
Deafness Sensorineural
|
Hearing Loss High-Frequency
|
|
Hearing Loss, Central
|
Hearing Loss, High-Frequency
|
|
|
| Colorectal Cancer |
|
Colon Cancer
|
Colorectal Carcinoma
|
|
Colon Carcinoma
|
Colorectal Cancer, Susceptibility To
|
|
Carcinoma Of Colon
|
CRC
|
|
Colorectal Cancer With Chromosomal Instability, Somatic
|
Colon Cancer, Somatic
|
|
Colon Cancer, Susceptibility To
|
Colonic Neoplasms
|
|
Colorectal Neoplasms
|
Colorectal Cancer, Somatic
|
|
Colon Cancer, Advanced, Somatic
|
Colonic Carcinoma
|
|
Colorectal Carcinomas
|
Colon Cancers
|
|
Colorectal Cancers
|
Cancer, Colorectal, Somatic
|
|
Cancer, Colon
|
Cancer, Colorectal, Susceptibility To
|
|
Colorectal Neoplasm
|
Colonic Neoplasm
|
|
Malignant Tumor Of Colon
|
|
|
| Goiter |
|
|
| Carney Complex Variant |
|
Carney Complex
|
Carney Syndrome
|
|
Carney Complex, Type 1
|
Lamb Syndrome
|
|
Name Syndrome
|
Myxoma-Spotty Pigmentation-Endocrine Overactivity Syndrome
|
|
Carney Complex - Trismus - Pseudocamptodactyly Syndrome
|
Carney Complex, Type 2
|
|
Car
|
Cnc1
|
|
Carney Myxoma-Endocrine Complex
|
Myxoma - Spotty Pigmentation - Endocrine Overactivity
|
|
Myxoma, Spotty Pigmentation, And Endocrine Overactivity
|
Lamb - Lentigines, Atrial Myxoma, Mucocutaneous Myoma, Blue Nevus Syndrome
|
|
Name - Nevi, Atrial Myxoma, Skin Myxoma, Ephelides Syndrome
|
Carney Complex-Trismus-Pseudocamptodactyly Syndrome
|
|
CACOV
|
|
|
| Conn'S Syndrome |
|
Cushing Syndrome
|
Hyperaldosteronism
|
|
Primary Hyperaldosteronism
|
Hypercortisolism
|
|
Primary Aldosteronism
|
Cushing'S Syndrome
|
|
Adrenal Gland Hyperfunction
|
Conn Syndrome
|
|
Hyperadrenalism
|
Ectopic Acth Syndrome
|
|
Hyperadrenocorticism
|
Cushing Disease
|
|
Adrenal Cortex Adenoma
|
Corticotroph Pituitary Adenoma
|
|
Cushing'S Disease
|
Pituitary Corticotroph Micro-Adenoma
|
|
Pituitary-Dependent Cushing Syndrome
|
Pituitary Acth Hypersecretion
|
|
Acth Syndrome, Ectopic
|
Acth-Secreting Pituitary Adenoma
|
|
Adrenal Hyperfunction Resulting From Pituitary Acth Excess
|
Ectopic Adrenocorticotropic Hormone Syndrome
|
|
Nodular Primary Adrenocortical Dysplasia
|
Pituitary Dependent Cushing Syndrome
|
|
Pituitary Cushing Syndrome
|
Pituitary-Dependant Cushing Syndrome
|
|
Pituitary-Dependant Hypercortisolism
|
Pituitary-Dependant Hypercortisolism Disorder
|
|
Aldosteronism Primary
|
Acth Syndrome Ectopic
|
|
Adrenal Cushing'S Syndrome
|
Adrenal Cortical Adenoma
|
|
Cushing Syndrome Nos
|
Cortisol Hypersecretion
|
|
Corticoadrenal Hypersecretion
|
Cushing Syndrome Secondary To Ectopic Acth-Secretion
|
|
Ectopic Cushing Syndrome
|
Hypercortisolism Due To Nonpituitary Tumour
|
|
Ectopic Acth - [Adrenocorticotropic Hormone] Secretion
|
Ectopic Acth - [Adrenocorticotropic Hormone] Secretion Causing Cushing Syndrome
|
|
Idiopathic Aldosteronism
|
Aldosteronism
|
|
Primary Aldosteronism Due To Bilateral Adrenal Hyperplasia
|
Primary Aldosteronism Due To Adrenal Hyperplasia
|
|
|
| Lymph Node Disease |
|
Abnormality Of The Lymph Nodes
|
Disorder Of Lymph Node
|
|
|
| Von Hippel-Lindau Syndrome |
|
Von Hippel-Lindau Disease
|
Vhl
|
|
Vhl Syndrome
|
VHLS
|
|
Von Hippel-Lindau Syndrome, Modifier Of
|
Hippel Lindau Syndrome
|
|
Angiomatosis Retinae
|
Cerebelloretinal Angiomatosis, Familial
|
|
Hippel-Lindau Disease
|
Familial Cerebelloretinal Angiomatosis
|
|
Lindau Disease
|
VHLD
|
|
|
| Paraganglioma And Gastric Stromal Sarcoma |
|
Carney-Stratakis Syndrome
|
Paraganglioma And Gastrointestinal Stromal Tumor
|
|
Carney Dyad
|
Carney-Stratakis Dyad Of Paraganglioma And Gastric Stromal Sarcoma
|
|
Paraganglioma And Gist
|
Carney-Stratakis Dyad
|
|
Gist-Paraganglioma Dyad
|
PGGSS
|
|
Paraganglioma, Gastric Stromal Sarcoma
|
Gastrointestinal Stromal Tumors
|
|
|
| Multiple Endocrine Neoplasia, Type I |
|
Multiple Endocrine Neoplasia Type 1
|
MEN1
|
|
Wermer Syndrome
|
Multiple Endocrine Neoplasia 1
|
|
Multiple Endocrine Neoplasia, Type 1
|
Men I
|
|
Endocrine Adenomatosis, Multiple
|
Mea I
|
|
Men Type I
|
Wermer'S Syndrome
|
|
Men1 Syndrome
|
Multiple Endocrine Adenomatosis
|
|
Endocrine Adenomatosis Multiple
|
Men 1
|
|
Familial Multiple Endocrine Neoplasia Type I
|
Neoplasia, Endocrine, Multiple, Type 1
|
|
Multiple Endocrine Neoplasia
|
|
|
| Inherited Cancer-Predisposing Syndrome |
|
Hereditary Cancer-Predisposing Syndrome
|
|
|
| Adrenal Medulla Cancer |
|
Adrenal Medulla Neoplasm
|
Adrenal Medulla Tumor
|
|
Malignant Neoplasm Of Adrenal Medulla
|
Malignant Tumor Of The Adrenal Medulla
|
|
Adrenal Medulla Carcinoma
|
Neoplasm Of Adrenal Medulla
|
|
|
| Primary Cutaneous Amyloidosis |
|
Plca
|
Primary Localized Cutaneous Amyloidosis
|
|
Familial Primary Localized Cutaneous Amyloidosis
|
Amyloidosis Ix
|
|
Lichen Amyloidosis Familial
|
Amyloidosis, Primary Cutaneous
|
|
Pca
|
Amyloidosis 9
|
|
Amyloidosis Familial Cutaneous Lichen
|
Fplca
|
|
Familial Lichen Amyloidosis
|
|
|
| Hypoparathyroidism |
|
Hypoparathyroidism, Idiopathic
|
Parathyroid, Underactivity Of
|
|
Syndrome With Hypoparathyroidism
|
Deficiency Of Parathyroid Hormone
|
|
Parathyroid Gland Insufficiency
|
Parathyroid Insufficiency
|
|
Hypoparathyroidism Due To Impaired Pth - [Parathyroid Hormone] Secretion
|
|
|
| Vesicoureteral Reflux |
|
|
| Congenital Mesoblastic Nephroma |
|
Nephroma, Mesoblastic
|
Mesoblastic Nephroma
|
|
|
| Sporadic Pheochromocytoma/Secreting Paraganglioma |
|
|
| Contractures, Pterygia, And Spondylocarpotarsal Fusion Syndrome 1a |
|
Multiple Pterygium Syndrome, Autosomal Dominant
|
CPSFS1A
|
|
Contractures, Pterygia, And Spondylocarpostarsal Fusion Syndrome 1a
|
Autosomal Dominant Disease
|
|
Contractures, Pterygia, And Variable Skeletal Fusions Syndrome 1a
|
Cpskf1a
|
|
Pterygium Syndrome, Multiple
|
Autosomal Dominant
|
|
Arthrogryposis, Distal, Type 8, Formerly
|
Da8, Formerly
|
|
Autosomal Dominant Multiple Pterygium Syndrome
|
Distal Arthrogryposis Type 8
|
|
Arthrogryposis, Distal, Type 8
|
Da8
|
|
Pterygium Syndrome, Multiple, Autosomal Dominant
|
Autosomal Dominant Disorder
|
|
|
| Inflammatory Myofibroblastic Tumor |
|
Inflammatory Fibrosarcoma
|
|
|
| Thyroid Gland Cancer |
|
Thyroid Gland Carcinoma
|
Malignant Neoplasm Of Thyroid Gland
|
|
Malignant Tumour Of Thyroid Gland
|
Thyroid Neoplasm
|
|
Thyroid Neoplasms
|
Neoplasm Of Thyroid Gland
|
|
Thyroid Gland Neoplasm
|
Head And Neck Cancer, Thyroid
|
|
Neoplasm Of The Thyroid Gland
|
Cancer Of The Thyroid
|
|
Primary Malignant Neoplasm Of Thyroglossal Duct
|
Malignant Neoplasm Of Thyroglossal Duct
|
|
Primary Malignant Neoplasm Of Thyroid Gland
|
Thyroglossal Duct Cancer
|
|
Toxic Goitre Malignant Tumour
|
Cancerous Goitre
|
|
|
| Congenital Fibrosarcoma |
|
|
| Megacolon |
|
|
| Nonsyndromic Paraganglioma |
|
Chemodectoma
|
Carotid Body Paraganglioma
|
|
Extra-Adrenal Paraganglioma
|
|
|
| Lung Cancer |
|
Lung Carcinoma
|
Non-Small Cell Lung Carcinoma
|
|
Lung Cancer, Protection Against
|
Lung Cancer, Susceptibility To
|
|
Adenocarcinoma Of Lung, Somatic
|
Nonsmall Cell Lung Cancer
|
|
Adenocarcinoma Of Lung, Response To Tyrosine Kinase Inhibitor In
|
Lung Neoplasm
|
|
Carcinoma Of Lung
|
Lung Non-Small Cell Carcinoma
|
|
Non-Small Cell Lung Cancer
|
Nsclc
|
|
Lung Neoplasms
|
Malignant Neoplasm Of Lung
|
|
Alveolar Cell Carcinoma
|
Nonsmall Cell Lung Cancer, Somatic
|
|
Nonsmall Cell Lung Cancer, Response To Tyrosine Kinase Inhibitor In
|
Nonsmall Cell Lung Cancer, Susceptibility To
|
|
Lung Cancer, Somatic
|
Lung Cancer, Resistance To
|
|
Cancer Of Lung
|
Cancer Of Bronchus
|
|
Cancer Of The Lung
|
Lung Malignancies
|
|
Lung Malignant Tumors
|
Malignant Lung Tumor
|
|
Malignant Tumor Of Lung
|
Pulmonary Cancer
|
|
Pulmonary Carcinoma
|
Pulmonary Neoplasms
|
|
Respiratory Carcinoma
|
LNCR
|
|
Adenocarcinoma Of Lung
|
Neoplasm Of Lung
|
|
Cancer Lung
|
Carcinoma Non-Small Cell Lung
|
|
Carcinoma, Non-Small-Cell Lung
|
Lung Cancers
|
|
Lung Carcinomas
|
Cancer, Lung
|
|
Cancer, Lung, Non-Small Cell
|
Primary Malignant Neoplasm Of Lung
|
|
Bronchioloalveolar Adenocarcinoma
|
|
|
| Breast Cancer |
|
Breast Carcinoma
|
Breast Cancer, Familial
|
|
Malignant Neoplasm Of Breast
|
Male Breast Cancer
|
|
Breast Cancer, Susceptibility To
|
Breast Cancer, Early-Onset
|
|
Malignant Tumor Of Breast
|
Carcinoma Of Male Breast
|
|
Breast Cancer, Invasive Ductal
|
Breast Cancer, Protection Against
|
|
Breast Cancer, Somatic
|
Breast Cancer, Male
|
|
Breast Cancer, Lobular, Somatic
|
Breast Tumor
|
|
Mammary Cancer
|
Mammary Tumor
|
|
Malignant Neoplasm Of Male Breast
|
Mammary Carcinoma
|
|
Male Breast Carcinoma
|
Familial Cancer Of Breast
|
|
Invasive Ductal Breast Carcinoma
|
Breast Cancer Susceptibility
|
|
Breast Cancer, Male, Susceptibility To
|
Breast Cancer, Early-Onset, Susceptibility To
|
|
Malignant Tumor Of The Breast
|
Mammary Neoplasm
|
|
Primary Breast Cancer
|
Neoplasm Of Male Breast
|
|
Carcinoma Of Breast
|
Breast Cancer In Men
|
|
Familial Breast Cancer
|
Cancer Of Breast
|
|
BC
|
Breast Cancer Familial
|
|
Breast Cancer Familial Male
|
Breast Cancer, Familial Male
|
|
Breast Male Carcinoma
|
Breast Neoplasms
|
|
Breast Neoplasms, Male
|
Mammary Tumors
|
|
Mammary Carcinomas
|
Cancer, Breast
|
|
Cancer, Breast, Susceptibility
|
Invasive Breast Ductal Carcinoma
|
|
Breast Neoplasm
|
Susceptibility To Breast Cancer
|
|
Mammary Neoplasms
|
Animal Mammary Neoplasms
|
|
Primary Malignant Neoplasm Of Breast
|
Infiltrating Ductal Carcinoma Of Breast
|
|
Infiltrating Duct Carcinoma Of Unspecified Site
|
Infiltrating Ductular Carcinoma Of Unspecified Site
|
|
Invasive Breast Carcinoma Of No Special Type
|
Microinvasive Carcinoma Of Breast
|
|
Carcinoma With Apocrine Differentiation
|
|
|
| Malignant Pheochromocytoma |
|
Pheochromocytoma, Malignant
|
|
|
| Lynch Syndrome |
|
Hereditary Nonpolyposis Colon Cancer
|
Hereditary Nonpolyposis Colorectal Cancer
|
|
Hereditary Nonpolyposis Colorectal Carcinoma
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
|
Familial Nonpolyposis Colon Cancer
|
Hnpcc
|
|
Coca 1
|
Hereditary Defective Mismatch Repair Syndrome
|
|
Hereditary Non-Polyposis Colon Cancer
|
Hereditary Non-Polyposis Colon Cancer Syndrome
|
|
Hereditary Non-Polyposis Colorectal Cancer
|
Hereditary Non-Polyposis Colorectal Cancer Syndrome
|
|
Hereditary Nonpolyposis Colon Cancer Syndrome
|
Hereditary Nonpolyposis Colorectal Cancer Syndrome
|
|
Hereditary Nonpolyposis Colorectal Neoplasm
|
Hnpcc - Hereditary Nonpolyposis Colon Cancer
|
|
Cancer Family Syndrome
|
Familial Nonpolyposis Colorectal Cancer
|
|
Colon Cancer, Familial Nonpolyposis
|
Colorectal Neoplasms, Hereditary Nonpolyposis
|
|
Cancer, Colorectal, Nonpolyposis, Hereditary
|
Colorectal Cancer, Hereditary Nonpolyposis, Type 1
|
|
|
| Multiple Mucosal Neuroma |
|
|
| Differentiated Thyroid Carcinoma |
|
Papillary Or Follicular Thyroid Carcinoma
|
Well-Differentiated Thyroid Carcinoma
|
|
Differentiated Thyroid Gland Carcinoma
|
|
|
| Charcot-Marie-Tooth Disease |
|
Cmt
|
Hmsn
|
|
Hereditary Motor And Sensory Neuropathy
|
Pma
|
|
Cmt - Charcot-Marie-Tooth Disease
|
Charcot Marie Tooth Disease
|
|
Charcot-Marie-Tooth Hereditary Neuropathy
|
Charcot-Marie-Tooth Syndrome
|
|
Peroneal Muscular Atrophy
|
Hereditary Motor And Sensory Neuropathies
|
|
|
| Intestinal Pseudo-Obstruction |
|
Chronic Intestinal Pseudoobstruction
|
Chronic Intestinal Pseudo-Obstruction
|
|
Cipo
|
Neuronal Intestinal Dysplasia
|
|
Hollow Visceral Myopathy
|
Familial Visceral Neuropathy
|
|
Paralytic Ileus
|
Intestinal Pseudoobstruction
|
|
Chronic Idiopathic Intestinal Pseudo-Obstruction
|
Ciip
|
|
Congenital Short Bowel Syndrome
|
Enteric Neuropathy
|
|
Familial Visceral Myopathy
|
Ipo
|
|
Pseudo-Obstruction Of Intestine
|
Pseudointestinal Obstruction Syndrome
|
|
Pseudoobstructive Syndrome
|
Congenital Idiopathic Intestinal Pseudoobstruction
|
|
Visceral Myopathy, Familial
|
|
|
| Lung Non-Squamous Non-Small Cell Carcinoma |
|
|
| Constipation |
|
|
| Salivary Gland Mucinous Adenocarcinoma |
|
|
| Amyloidosis |
|
Amyloid Disease
|
Amyloid
|
|
Amyloid Degeneration
|
Amyloidosis Nos
|
|
Amyloid Deposition
|
Amyloid Infiltration
|
|
Idiopathic Amyloidosis
|
Hyaloid Degeneration
|
|
Lardaceous Degeneration
|
|
|
| Cardiovascular Organ Benign Neoplasm |
|
|
| Waardenburg Syndrome, Type 4a |
|
Waardenburg-Shah Syndrome
|
Shah-Waardenburg Syndrome
|
|
Waardenburg Syndrome Type 4a
|
WS4A
|
|
Ws4
|
Waardenburg Syndrome Type 4
|
|
Waardenburg Syndrome Type Iva
|
Waardenburg Syndrome With Hirschsprung Disease Type 4a
|
|
Hirschsprung Disease With Pigmentary Anomaly
|
Waardenburg-Hirschsprung Syndrome
|
|
Waardenburg Syndrome, Type Iva
|
Waardenburg Syndrome With Hirschsprung Disease, Type 4a
|
|
Waardenburg-Hirschsprung Disease
|
Waardenburg Syndrome, Type 4
|
|
Waardenburg Syndrome 4a
|
|
|
| Tumor Predisposition Syndrome |
|
TPDS
|
Tumor Predisposition
|
|
|
| Hypermobile Ehlers-Danlos Syndrome |
|
Heds
|
Ehlers-Danlos Syndrome Type 3
|
|
Ehlers-Danlos Syndrome Hypermobility Type
|
Hypermobile Eds
|
|
Joint Hypermobility
|
Benign Joint Hypermobility Syndrome
|
|
Eds Hypermobility Type
|
Eds Type Iii
|
|
Ehlers-Danlos Syndrome Type Iii
|
Joint Hypermobility Syndrome
|
|
Eds3
|
Ehlers-Danlos Syndrome, Hypermobility Type
|
|
Eds Iii
|
Eds-Ht
|
|
|
| Hypothyroidism |
|
Thyroid Diseases
|
Thyroid Deficiency
|
|
Thyroid Insufficiency
|
Dysfunction Thyroid
|
|
Thyroid Disease
|
Thyroid Dysfunction
|
|
|
| Parathyroid Adenoma |
|
Adenoma Of Parathyroid
|
Adenoma Of The Parathyroid Gland
|
|
Parathyroid Gland Adenoma
|
|
|
| Neurofibromatosis, Type I |
|
Von Recklinghausen Disease
|
Neurofibromatosis 1
|
|
Neurofibromatosis, Type 1
|
NF1
|
|
Neurofibromatosis, Peripheral Type
|
Neurofibromatosis Type I
|
|
Neurofibromatosis Type 1 Due To Nf1 Mutation Or Intragenic Deletion
|
Familial Spinal Neurofibromatosis
|
|
Fsnf
|
Peripheral Neurofibromatosis
|
|
Von Recklinghausen'S Neurofibromatosis
|
Von Recklinghausen Disease Due To Nf1 Mutation Or Intragenic Deletion
|
|
Neurofibromatosis Peripheral Type
|
Von Recklinghausen Syndrome
|
|
Neurofibromatosis Type 1
|
Von Recklinghausen Neuropathy
|
|
Nf1 - [Neurofibromatosis Type 1]
|
Recklinghausen Disease
|
|
|
| Main Bronchus Cancer |
|
Malignant Neoplasm Of Main Bronchus
|
Ca Main Bronchus
|
|
|
| Renal Cell Carcinoma, Papillary, 1 |
|
Papillary Renal Cell Carcinoma
|
Hereditary Papillary Renal Cell Carcinoma
|
|
Papillary Renal Cell Carcinoma, Sporadic
|
Papillary Renal Cell Adenocarcinoma
|
|
RCCP
|
RCCP1
|
|
Renal Cell Carcinoma, Papillary
|
Renal Cell Carcinoma, Papillary, 1, Familial And Somatic
|
|
Chromophil Carcinoma Of Kidney
|
Papillary Kidney Carcinoma
|
|
Sporadic Papillary Renal Cell Carcinoma
|
Chromophil Renal Cell Carcinoma
|
|
Papillary Renal Carcinoma, Malignant -
|
Papillary Renal Cell Carcinoma, Bilateral -
|
|
Papillary Renal Cell Carcinoma, Familial -
|
Papillary Renal Cell Carcinoma, Multiple -
|
|
Papillary Renal Cell Carcinoma, Sporadic -
|
Renal Adenocarcinoma
|
|
Chromophil Rcc
|
Hprcc
|
|
Renal Cell Carcinoma Papillary
|
Chromophilic Renal Cell Carcinoma
|
|
Prcc
|
Carcinoma, Renal Cell, Papillary, Type 1
|
|
Type 1 Papillary Renal Cell Carcinoma
|
Renal Cell Carcinoma
|
|
Hereditary Papillary Renal Carcinoma
|
|
|
| Pyloric Stenosis |
|
|
| Renal Hypodysplasia/Aplasia 1 |
|
Renal Agenesis
|
Renal Adysplasia
|
|
Renal Aplasia
|
RHDA1
|
|
Hereditary Renal Aplasia
|
Hra
|
|
Hereditary Urogenital Adysplasia
|
Hypodysplasia/Aplasia, Renal, Type 1
|
|
Congenital Absence Of Kidneys Syndrome
|
Congenital Absence Of Kidney
|
|
Aplastic Kidney
|
|
|
| Cowden Syndrome |
|
Cowden Disease
|
Multiple Hamartoma Syndrome
|
|
Cowden'S Disease
|
Lhermitte-Duclos Disease
|
|
Cd
|
Cs
|
|
Mham
|
Dysplastic Gangliocytoma Of Cerebellum
|
|
Cowden'S Syndrome
|
Hamartoma Syndrome, Multiple
|
|
|
| Multiple Endocrine Neoplasia |
|
Men
|
Multiple Endocrine Adenomatosis
|
|
Multiple Endocrine Neoplasia Syndrome
|
Adenomatosis, Familial Endocrine
|
|
Endocrine Neoplasia, Multiple
|
Familial Endocrine Adenomatosis
|
|
Mea
|
Multiple Endocrine Neoplasms
|
|
Multiple Endocrine Neoplasia Type 1
|
|
|
| Malignant Struma Ovarii |
|
|
| Spinocerebellar Ataxia, Autosomal Recessive 3 |
|
SCAR3
|
Scabd
|
|
Autosomal Recessive Spinocerebellar Ataxia Type 3
|
Autosomal Recessive Spinocerebellar Ataxia-Blindness-Deafness Syndrome
|
|
Autosomal Recessive Spinocerebellar Ataxia-Blindness-Hearing Loss Syndrome
|
Spinocerebellar Ataxia With Blindness And Deafness
|
|
Autosomal Recessive Spinocerebellar Ataxia 3
|
Spinocerebellar Ataxia Autosomal Recessive 3
|
|
Autosomal Recessive Cerebellar Ataxia - Blindness - Deafness
|
Autosomal Recessive Cerebellar Ataxia-Blindness-Deafness Syndrome
|
|
|
| Autosomal Genetic Disease |
|
Autosomal Hereditary Disorder
|
|
|
| Nodular Goiter |
|
Goiter, Nodular
|
Nodular Goitre
|
|
Goiter Nodular
|
Non-Toxic Nodular Goiter
|
|
|
| Adenoma |
|
Acinar Cell Adenoma
|
Adenomas
|
|
Acinic Cell Adenoma
|
|
|
