| Diseases |
Alias |
|
| Hirschsprung Disease 3 |
|
Hirschsprung Disease, Susceptibility To, 3
|
HSCR3
|
|
Hirschsprung Disease Type 3
|
Hirschsprung Disease Modifier
|
|
Hirschsprung Disease, Type 3
|
|
|
| Spinal Cord Injury |
|
|
| 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
|
|
|
| Spinal Cord Disease |
|
Spinal Cord Diseases
|
Myelopathy
|
|
Bone Marrow Diseases
|
|
|
| Intestinal Obstruction |
|
Inspissated Milk Syndrome
|
Milk Curd Syndrome
|
|
|
| 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
|
|
|
| Neuroma |
|
|
| Hirschsprung Disease 1 |
|
Hirschsprung Disease
|
Aganglionic Megacolon
|
|
Hscr
|
Hirschsprung'S Disease
|
|
Congenital Megacolon
|
Congenital Intestinal Aganglionosis
|
|
Colonic Aganglionosis
|
Hirschsprung Disease, Susceptibility To, 1
|
|
Hirschsprung Disease, Protection Against
|
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 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
|
Pheochromocytoma And Amyloid Producing Medullary Thyroid Carcinoma
|
|
Multiple Endocrine Neoplasia, Type 2a
|
Pheochromocytoma And Amyloid-Producing Medullary Thyroid Carcinoma
|
|
Multiple Endocrine Neoplasia Ii
|
Men2 Syndrome
|
|
Men-2a Syndrome
|
Multiple Neoplasia 2a
|
|
Multiple Neoplasia Type 2
|
|
|
| Thyroid Carcinoma, Familial Medullary |
|
Medullary Thyroid Carcinoma
|
Familial Medullary Thyroid Carcinoma
|
|
MTC
|
Medullary Thyroid Cancer
|
|
Fmtc
|
Mtc1
|
|
Thyroid Cancer, Medullary
|
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
|
|
|
| Constipation |
|
|
| 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
|
|
|
| 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
|
|
|
| Goldberg-Shprintzen Syndrome |
|
Goldberg-Shprintzen Megacolon Syndrome
|
GOSHS
|
|
Megacolon-Microcephaly Syndrome
|
|
|
| Diabetic Neuropathy |
|
|
| 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
|
|
|
| Parkinson Disease, Late-Onset |
|
Parkinson Disease
|
Parkinson'S Disease
|
|
PD
|
PARK
|
|
Parkinson Disease, Susceptibility To
|
Late Onset Parkinson'S Disease
|
|
Late Onset Parkinson Disease
|
Paralysis Agitans
|
|
Primary Parkinsonism
|
Idiopathic Parkinson Disease
|
|
Parkinson'S
|
Parkinson Disease, Late-Onset, Susceptibility To
|
|
Parkinson Disease, Age Of Onset, Modifier
|
Lewy Body Parkinson Disease
|
|
Idiopathic Parkinson'S Disease
|
Pd - [Parkinson Disease]
|
|
Parkinson Disease Nos
|
Parkinson, Nos
|
|
Primary Parkinson Disease
|
|
|
| Parkinsonism |
|
Parkinsonism-Plus
|
Idiopathic Parkinsonism
|
|
Primary Parkinsonism
|
Paralysis Agitans Syndrome
|
|
Parkinsonian Syndrome
|
Trembling Paralysis
|
|
Paralysis Agitans
|
Shaking Palsy
|
|
Shaking Paralysis
|
|
|
| Brachial Plexus Lesion |
|
Brachial Plexus Injuries
|
Brachial Plexus Lesions
|
|
|
| Neuritis |
|
|
| Meningoencephalitis |
|
Acquired Toxoplasmal Meningoencephalitis
|
Meningoencephalitis Due To Acquired Toxoplasmosis
|
|
Meningoencephalitis Due To Toxoplasmosis
|
Toxoplasma Meningoencephalitis
|
|
|
| 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
|
|
|
| Pyloric Stenosis |
|
|
| Major Depressive Disorder |
|
Seasonal Affective Disorder
|
Unipolar Depression
|
|
Depression
|
MDD
|
|
Depressive Disorder
|
Unipolar Depression, Susceptibility To
|
|
Major Depressive Disorder 1
|
Major Depressive Disorder, Response To Citalopram Therapy In
|
|
Major Depressive Disorder 2
|
Winter Depression
|
|
Single Major Depressive Episode
|
Sad
|
|
Clinical Depression
|
Major Depression
|
|
Depressive Syndrome
|
Major Depressive Disorder And Accelerated Response To Antidepressant Drug Treatment
|
|
Seasonal Affective Disorder, Susceptibility To
|
Recurrent Major Depression
|
|
Affective Disorder, Seasonal
|
Depression In A Seasonal Pattern
|
|
Depression
|
Seasonal
|
|
Major Depressive Disorder With A Seasonal Pattern
|
Seasonal Depression
|
|
Seasonal Mood Disorder
|
Mental Depression
|
|
Recurrent Major Depressive Episodes
|
|
|
| Retinal Degeneration |
|
|
| Jejunoileitis |
|
|
| Polyneuropathy |
|
|
| Meningitis |
|
Streptococcal Meningitis
|
Acute Streptococcal Meningitis
|
|
Staphylococcal Meningitis
|
Adenoviral Meningitis
|
|
Influenza Meningitis
|
Influenzal Meningitis
|
|
Meningitis Due To H. Influenzae
|
Cryptococcal Meningitis
|
|
Fungal Meningitis Due To Cryptococcus Neoformans
|
Cryptococcosis Meningitis
|
|
Cryptococcus Meningitis
|
Cryptococcal Meningoencephalitis
|
|
Meningitis Due To Cryptococcus
|
Mumps Virus Meningitis
|
|
Mumps Meningitis
|
|
|
| Urinary Tract Obstruction |
|
Obstructive Uropathy
|
Urinary Obstruction
|
|
Urologic Diseases
|
|
|
| Amyotrophic Lateral Sclerosis 1 |
|
Amyotrophic Lateral Sclerosis
|
ALS
|
|
Lou Gehrig Disease
|
Amyotrophic Lateral Sclerosis Type 1
|
|
Charcot Disease
|
ALS1
|
|
Amyotrophic Lateral Sclerosis, Susceptibility To
|
Fals
|
|
Lou Gehrig'S Disease
|
Mnd
|
|
Motor Neuron Disease
|
Familial Amyotrophic Lateral Sclerosis
|
|
Amyotrophic Lateral Sclerosis 1, Familial
|
Amyotrophic Lateral Sclerosis 1, Autosomal Dominant
|
|
Motor Neuron Disease, Bulbar
|
Motor Neurone Disease
|
|
Amyotrophic Lateral Sclerosis With Dementia
|
Dementia With Amyotrophic Lateral Sclerosis
|
|
Motor Neuron Disease, Amyotrophic Lateral Sclerosis
|
Sclerosis, Lateral, Amyotrophic
|
|
Sclerosis, Lateral, Amyotrophic, Type 1
|
Amyotrophic Sclerosis
|
|
Als - [Amyotrophic Lateral Sclerosis]
|
Wasting Palsy
|
|
Amyotrophic Paralysis
|
Amyotrophy Lateral Sclerosis
|
|
Wasting Paralysis
|
Spinal Progressive Amyotrophy
|
|
Progressive Atrophic Paralysis
|
|
|
| Common Peroneal Nerve Lesion |
|
Lesion Of Lateral Popliteal Nerve
|
Fibular Neuropathy
|
|
|
| Tetanus |
|
Lockjaw
|
Clostridial Tetanus
|
|
Infection Due To Clostridium Tetani
|
Lock-Jaw
|
|
|
| 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
|
|
|
| Papillorenal Syndrome |
|
Renal Coloboma Syndrome
|
Coloboma Of Optic Nerve With Renal Disease
|
|
Renal-Coloboma Syndrome
|
Optic Nerve Coloboma With Renal Disease
|
|
Optic Coloboma, Vesicoureteral Reflux, And Renal Anomalies
|
Renal-Coloboma Syndrome With Macular Abnormalities
|
|
Congenital Anomalies Of The Kidney And Urinary Tract With Or Without Ocular Abnormalities
|
Cakut With Or Without Ocular Abnormalities
|
|
PAPRS
|
Optic Coloboma, Vesicoureteral Reflux And Renal Anomalies
|
|
Papillo-Renal Syndrome, Optic Nerve Coloboma With Renal Disease
|
Coloboma-Ureteral-Renal Syndrome
|
|
Oncr
|
Optic Nerve Coloboma Renal Syndrome
|
|
Rcs
|
Papillo-Renal Syndrome
|
|
Optic Coloboma Vesicoureteral Reflux And Renal Anomalies
|
|
|
| Multiple System Atrophy 1 |
|
Multiple System Atrophy
|
Shy-Drager Syndrome
|
|
Msa
|
MSA1
|
|
Multiple System Atrophy 1, Susceptibility To
|
Sporadic Olivopontocerebellar Atrophy
|
|
Multisystem Atrophy
|
Msa1, Susceptibility To
|
|
Multiple System Atrophy, Susceptibility To
|
Opca
|
|
Progressive Autonomic Failure With Multiple System Atrophy
|
Sds
|
|
|
| Megacolon |
|
|
| Paralytic Lagophthalmos |
|
|
| Multiple Mucosal Neuroma |
|
|
| Renal Hypoplasia |
|
|
| 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
|
|
|
| Focal Hand Dystonia |
|
Organic Writer'S Cramp
|
Dystonia, Focal, Task-Specific
|
|
|
| Bipolar Disorder |
|
Bipolar Depression
|
Manic Disorder
|
|
Depression, Bipolar
|
Bipolar Disorder Manic Phase
|
|
Depressive-Manic Psych.
|
Manic Bipolar Affective Disorder
|
|
Manic Bipolar I Disorder
|
Manic Depression
|
|
Manic Depressive Disorder
|
Mixed Bipolar Disorder
|
|
Bipolar Affective Disorder
|
Bipolar Affective Psychosis
|
|
Bipolar Spectrum Disorder
|
Manic Depressive Illness
|
|
Depression Bipolar
|
Bipolar Disorder, Mixed
|
|
Major Affective Disorder
|
Major Affective Disorder 1
|
|
Major Affective Disorder 2
|
|
|
| Narcolepsy |
|
Paroxysmal Sleep
|
Gelineau Syndrome
|
|
Narcoleptic Syndrome
|
Narcolepsy-Cataplexy Syndrome
|
|
Cataplexy And Narcolepsy
|
Narcolepsy, Without Cataplexy
|
|
Gelineau'S Syndrome
|
Narcolepsy With Or Without Cataplexy
|
|
Narcolepsy Nos
|
|
|
| Rett Syndrome |
|
Atypical Rett Syndrome
|
RTT
|
|
Rett Disorder
|
Rts
|
|
Autism, Dementia, Ataxia, And Loss Of Purposeful Hand Use
|
Rett Syndrome, Preserved Speech Variant
|
|
Rett Syndrome, Atypical
|
Rett'S Disorder
|
|
Rett Syndrome Variant
|
Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use Syndrome
|
|
Cerebroatrophic Hyperammonemia
|
Rett Like Syndrome
|
|
Rett'S Syndrome
|
Atypical Rtt
|
|
Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use
|
Rett Syndrome Preserved Speech Variant
|
|
Rett Syndrome Zappella Variant
|
Rett Syndrome, Zappella Variant
|
|
|
| Intraocular Pressure Quantitative Trait Locus |
|
Glaucoma
|
IOPQTL
|
|
Glaucoma, Susceptibility To
|
Postinfectious Glaucoma
|
|
Glaucoma With Ocular Inflammation
|
Glaucoma Secondary To Eye Inflammation
|
|
Traumatic Glaucoma
|
Glaucoma With Concussion Of Globe
|
|
Glaucoma Due To Ocular Trauma
|
Glaucoma Associated With Ocular Trauma
|
|
Glaucoma Secondary To Drugs
|
|
|
| Thyroid Gland Medullary Carcinoma |
|
Medullary Thyroid Carcinoma
|
Medullary Carcinoma Of The Thyroid Gland
|
|
Ultimobranchial Thyroid Tumor
|
Ultimobranchial Thyroid Tumour
|
|
Thyroid Cancer, Medullary
|
|
|
| Pancreatic Cancer |
|
Pancreatic Carcinoma
|
Carcinoma Of Pancreas
|
|
Familial Pancreatic Carcinoma
|
Pancreatic Neoplasm
|
|
Pancreatic Carcinoma, Familial
|
Malignant Neoplasm Of Pancreas
|
|
Pancreatic Acinar Carcinoma
|
Pancreatic Tumor
|
|
Familial Pancreatic Cancer
|
Neoplasm Of The Pancreas
|
|
Cancer 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
|
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
|
|
|
| Striatonigral Degeneration |
|
|
| Hydrocephalus |
|
Hydrocephalus, Nonsyndromic, Autosomal Recessive
|
Hydrocephalus, X-Linked
|
|
Hydrocephalus Adverse Event
|
Hydrocephaly Nos
|
|
|
| Acoustic Neuroma |
|
Neurofibromatosis Type 2
|
Vestibular Schwannoma
|
|
Acoustic Neurinoma
|
Bilateral Acoustic Neurofibromatosis
|
|
Nf2
|
Acoustic Neurilemoma
|
|
Cerebellopontine Angle Tumor
|
Neurofibromatosis Central Type
|
|
Neurofibromatosis Type Ii
|
Vestibular Neurilemmoma
|
|
Acoustic Tumor
|
Neurinoma Of The Acoustic Nerve
|
|
Acoustic Neurinoma Bilateral
|
Acoustic Schwannomas Bilateral
|
|
Banf
|
Central Neurofibromatosis
|
|
Familial Acoustic Neuromas
|
Neurofibromatosis 2
|
|
Neurofibromatosis Type 2 Merlin
|
Schwannoma, Acoustic, Bilateral
|
|
Neuroma Acoustic
|
Neuroma, Acoustic
|
|
Familial Acoustic Neuroma
|
Familial Vestibular Schwannoma
|
|
Neurofibromatosis, Central Type
|
Nf2 - [Neurofibromatosis Type 2]
|
|
|
| Anxiety |
|
Anxiety Disorder
|
Anxiety Disorders
|
|
Anxiety State
|
Anxieties
|
|
Anxiety Neurosis
|
|
|
| Toxic Encephalopathy |
|
Neurotoxicity
|
Neurotoxicity Syndromes
|
|
Neurotoxicity Syndrome
|
Encephalopathy, Toxic
|
|
|
| Mood Disorder |
|
Mood Disorders
|
Episodic Mood Disorder
|
|
|
| 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
|
|
|
| Neuromuscular Disease |
|
Neuromuscular Diseases
|
Neuromuscular Disorders
|
|
Neuromuscular Disorder
|
|
|
| Cerebral Artery Occlusion |
|
|
| Stroke, Ischemic |
|
Cerebral Infarction
|
Stroke
|
|
Ischemic Stroke
|
Cerebrovascular Accident
|
|
Cerebral Infarction, Susceptibility To
|
Stroke, Ischemic, Susceptibility To
|
|
Cerebral Infarct
|
Ischemic Stroke, Susceptibility To
|
|
Stroke, Susceptibility To
|
Cva - Cerebral Infarction
|
|
ISCHSTR
|
Ischemic Cerebrovascular Accident
|
|
|
| Spondylometaphyseal Dysplasia With Corneal Dystrophy |
|
SMDCD
|
Spondylometaphyseal Dysplasia-Corneal Dystrophy Syndrome
|
|
Smd-Corneal Dystrophy Syndrome
|
|
|
| Schizophrenia |
|
SCZD
|
Schizophrenia With Or Without An Affective Disorder
|
|
Schizophrenia 12
|
Schizophrenia, Susceptibility To
|
|
Schizophrenia-1
|
Dementia Praecox
|
|
Schizophrenia 1
|
|
|
| Spinal Muscular Atrophy |
|
Sma
|
5q Sma
|
|
Proximal Sma
|
Sma-Associated Sma
|
|
Spinal Amyotrophies
|
Spinal Amyotrophy
|
|
Spinal Muscle Degeneration
|
Spinal Muscle Wasting
|
|
Muscular Atrophy Spinal
|
Atrophy, Muscular, Spinal
|
|
Hereditary Motor Neuronopathy
|
Progressive Muscular Atrophy
|
|
Sma - [Spinal Muscular Atrophy]
|
|
|
| Vesicoureteral Reflux |
|
|
| Febrile Seizures, Familial, 1 |
|
FEB1
|
Convulsions, Familial Febrile, 1
|
|
Familial Febrile Seizures 1
|
Familial Febrile Convulsions 1
|
|
|
| Neuroblastoma |
|
Nb
|
Neuroblastoma, Susceptibility To
|
|
Neuroblastomas
|
Central Neuroblastoma
|
|
|
| Heart Disease |
|
Heart Failure
|
Congenital Heart Disease
|
|
Heart Diseases
|
Congenital Heart Defects
|
|
Congenital Heart Defect
|
Heart Malformation
|
|
Congenital Anomaly Of Heart
|
Heart Defect
|
|
Heart-Congenital Defect
|
Congenital Heart Disorder
|
|
Heart Defects Congenital
|
Heart Defects, Congenital
|
|
Heart Defects
|
Heart Disease, Congenital
|
|
Disease, Heart, Congenital
|
Congestive Heart Failure
|
|
|
| Alzheimer Disease, Familial, 1 |
|
Alzheimer Disease
|
Alzheimer'S Disease
|
|
Presenile And Senile Dementia
|
AD1
|
|
Alzheimer Disease, Susceptibility To
|
Alzheimer Disease, Late-Onset, Susceptibility To
|
|
Alzheimer Disease 1, Familial
|
AD
|
|
Familial Alzheimer Disease
|
Alzheimer Disease, Late-Onset
|
|
Alzheimers Dementia
|
Alzheimer Dementia
|
|
Alzheimer Sclerosis
|
Alzheimer Syndrome
|
|
Alzheimer-Type Dementia
|
Dat
|
|
Primary Senile Degenerative Dementia
|
Sdat
|
|
Alzheimer Disease 1
|
Autosomal Dominant Alzheimer Disease
|
|
Early-Onset Alzheimer Disease With Cerebral Amyloid Angiopathy
|
Late Onset Alzheimer Disease
|
|
Alzheimers Disease
|
Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy
|
|
Late-Onset Alzheimers Disease
|
Alzheimer'S Disease Pathway Kegg
|
|
Dementia Due To Alzheimer'S Disease
|
Alzheimer Disease Type 1
|
|
Alzheimers
|
|
|
| Huntington Disease |
|
Huntington'S Disease
|
Huntington Chorea
|
|
Huntington'S Chorea
|
HD
|
|
Huntington Chronic Progressive Hereditary Chorea
|
Juvenile Huntington Disease
|
|
Chronic Progressive Chorea
|
Chronic Progressive Hereditary Chorea
|
|
Hc - [Huntington Chorea]
|
Hereditary Chorea
|
|
Progressive Hereditary Chorea
|
|
|
| Movement Disease |
|
Movement Disorders
|
Movement Disorder
|
|
|
| Spermatogenic Failure |
|
Azoospermia
|
Spgf
|
|
Spermatogenic Failure, Susceptibility To
|
Absent Sperm
|
|
Aspermatogenesis
|
Infertility Due To Azoospermia
|
|
Hypospermatogenesis
|
Azoospermatism
|
|
|
| Microcephaly |
|
Microencephaly
|
Microcephalus
|
|
Microcephalic
|
Nanocephaly
|
|
Congenital Microcephaly
|
Brain Hypoplasia
|
|
Brain Nondevelopment
|
Cephalic Hypoplasia
|
|
Undeveloped Cerebrum
|
Undeveloped Brain
|
|
Micrencephalon
|
Micrencephaly
|
|
|
| Peripheral Nervous System Disease |
|
Peripheral Neuropathy
|
Peripheral Nerve Disease
|
|
Peripheral Nerve Disorders
|
Neuropathy, Peripheral
|
|
Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation
|
|
|
| Polycystic Kidney Disease |
|
Polycystic Kidney Diseases
|
Pkd
|
|
Polycystic Renal Disease
|
Kidney Disease, Polycystic
|
|
Polycystic Kidney, Autosomal Dominant
|
|
|
| Cryptorchidism, Unilateral Or Bilateral |
|
Cryptorchidism
|
Undescended Testicle
|
|
Undescended Testis
|
Cryptorchism
|
|
Undescended Testicles
|
CRYPTO
|
|
Impaired Testicular Descent
|
Cryptosporidiosis
|
|
Retained Testis
|
Unilateral Cryptorchidism
|
|
Unilateral Undescended Testis
|
Nondescent Unilateral Testicle
|
|
Unilateral Cryptorchism
|
Ectopic Testis, Unilateral
|
|
Bilateral Cryptorchidism
|
Bilateral Cryptorchism
|
|
Bilateral Nondescent Testicle
|
Bilateral Undescended Testes
|
|
Bilateral Ectopic Testes
|
|
|
| Nervous System Disease |
|
Abnormality Of The Nervous System
|
Nervous System Diseases
|
|
Nervous System Disorder
|
|
|
| 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
|
|
|
| Attention Deficit-Hyperactivity Disorder |
|
Attention Deficit Hyperactivity Disorder
|
ADHD
|
|
Attention Deficit Disorder
|
Attention Deficit-Hyperactivity Disorder, Susceptibility To
|
|
Attention Deficit Disorder With Hyperactivity
|
Hyperkinetic Disorder
|
|
Hyperactivity Of Childhood
|
Attention-Deficit/Hyperactivity Disorder
|
|
Add
|
Addh
|
|
Attention Deficit
|
Attention Deficit Disorder Of Childhood With Hyperactivity
|
|
Attention Deficit Disorder With Hyperactivity Syndrome
|
Hyperkinetic Syndrome
|
|
Attention-Deficit Hyperactivity Disorder
|
Attention-Deficit/Hyperactivity Disorder, Predominantly Inattentive Type
|
|
Disturbance Of Activity And Attention
|
Disorder Of Activity And Attention
|
|
Adhd - [Attention Deficit Hyperactivity Disorder]
|
Hyperkinetic Disorders
|
|
Disorder Of Activity And Attention With Hyperkinesia
|
Attention Deficit Syndrome With Hyperactivity
|
|
|
| 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
|
|
|
| Eye Disease |
|
Eye Diseases
|
Abnormality Of The Eye
|
|
Toxoplasma Oculopathy
|
|
|
| Leber Plus Disease |
|
Leber Congenital Amaurosis
|
Lca
|
|
Leber'S Amaurosis
|
Leber'S Disease
|
|
Amaurosis Congenita Of Leber
|
Amaurosis Congenita Of Leber, Type 1
|
|
Lhon Plus Disease
|
Congenital Absence Of The Rods And Cones
|
|
Congenital Retinal Blindness
|
Crb
|
|
Congenital Amaurosis Of Retinal Origin
|
Leber'S Congenital Amaurosis
|
|
Leber Congenital Amaurosis 1
|
Leber'S Congenital Tapetoretinal Degeneration
|
|
Leber'S Congenital Tapetoretinal Dysplasia
|
Lca1
|
|
Leber Congenital Amaurosis Type 1
|
Retinal Blindness, Congenital
|
|
Amaurosis, Leber Congenital
|
Dysgenesis Neuroepithelialis Retinae
|
|
Hereditary Epithelial Dysplasia Of Retina
|
Hereditary Retinal Aplasia
|
|
Heredoretinopathia Congenitalis
|
Leber Abiotrophy
|
|
Leber Congenital Tapetoretinal Degeneration
|
Lebers Congenital Amaurosis
|
|
Optic Atrophy, Hereditary, Leber
|
|
|
| Fundus Dystrophy |
|
Retinal Dystrophy
|
Retinal Dystrophies
|
|
Dystrophy, Retinal
|
|
|
