| Diseases |
Alias |
|
| 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
|
|
|
| Hemolytic Anemia |
|
Anemia, Hemolytic
|
Anemia Hemolytic
|
|
Anaemia Due To Other Disorders Of Glutathione Metabolism
|
Chronic Non Spherocytic Anaemia
|
|
G6pd - [Glucose-6-Phosphate Dehydrogenase Deficiency] Anaemia
|
Anaemia Due To Glucose-6-Phosphate Dehydrogenase Deficiency
|
|
Glucose-6-Phosphate Dehydrogenase Deficiency With Anaemia
|
Glucose-6-Phosphate Dehydrogenase Deficiency Anaemia
|
|
Favism Anaemia
|
Haemolytic Anaemia Due Tog6pd Deficiency
|
|
Favism
|
Pentose Phosphate Pathway Disorder Anaemia
|
|
Anaemia Due To Pentose Phosphate Pathway Defect
|
|
|
| Alternating Hemiplegia Of Childhood |
|
Alternating Hemiplegia
|
Ahc
|
|
Alternating Hemiplegia Syndrome
|
Hemiplegia, Alternating, Of Childhood
|
|
Hemiplegia, Crossed
|
|
|
| Hemangioma |
|
|
| Dystonia 9 |
|
DYT9
|
Choreoathetosis/Spasticity, Episodic
|
|
Episodic Choreoathetosis/Spasticity
|
Cse Choreoathetosis, Paroxysmal, With Episodic Ataxia
|
|
Choreoathetosis, Kinesigenic, With Episodic Ataxia And Spasticity
|
Paroxysmal Dystonic Choreathetosis With Episodic Ataxia And Spasticity
|
|
Cse
|
Dystonia-9
|
|
Kinesigenic Choreoathetosis With Episodic Ataxia And Spasticity
|
Paroxysmal Choreoathetosis With Episodic Ataxia
|
|
Dystonia, Type 9
|
|
|
| Microvascular Complications Of Diabetes 5 |
|
Diabetic Retinopathy
|
Microvascular Complications Of Diabetes, Susceptibility To, 5
|
|
MVCD5
|
Retinopathy, Diabetic
|
|
Diabetic Nephropathy
|
Retinopathy, Diabetic, Susceptibility To
|
|
Retinal Abnormality - Diabetes-Related
|
|
|
| Dystonia |
|
Dystonic Disease
|
Dystonic Disorder
|
|
Dystonia Disorders
|
Neuroleptic Dyskinesia
|
|
|
| Spastic Paraplegia 9b, Autosomal Recessive |
|
SPG9B
|
Autosomal Recessive Complex Spastic Paraplegia Type 9b
|
|
Hereditary Spastic Paraplegia 9b
|
Autosomal Recessive Spastic Paraplegia 9b
|
|
Autosomal Recessive Spastic Paraplegia Type 9b
|
Ar-Spg9b
|
|
|
| Rapidly Involuting Congenital Hemangioma |
|
|
| Schizophrenia |
|
SCZD
|
Schizophrenia With Or Without An Affective Disorder
|
|
Schizophrenia 12
|
Schizophrenia, Susceptibility To
|
|
Schizophrenia-1
|
Dementia Praecox
|
|
Schizophrenia 1
|
|
|
| Hemangioblastoma |
|
Capillary Hemangioblastoma
|
|
|
| Epilepsy, Myoclonic Juvenile |
|
Juvenile Myoclonic Epilepsy
|
Janz Syndrome
|
|
Jme
|
Myoclonic Epilepsy, Juvenile, Susceptibility To, 1
|
|
EJM
|
Myoclonic Epilepsy, Juvenile
|
|
Petit Mal, Impulsive
|
Myoclonic Epilepsy, Juvenile 1
|
|
Myoclonic Epilepsy, Juvenile, 1
|
Adolescent Myoclonic Epilepsy
|
|
Juvenile Myoclonus Epilepsy
|
Juvenile Myoclonic Epilepsy 1
|
|
EJM1
|
Petit Mal Impulsive
|
|
Susceptibility To Juvenile Myoclonic Epilepsy 1
|
Myoclonic Epilepsy Juvenile
|
|
Epilepsy, Myoclonic, Juvenile
|
Myoclonic Epilepsy Of Janz
|
|
Jme - [Juvenile Myoclonic Epilepsy]
|
|
|
| Hyperinsulinism |
|
|
| Hemangioma Of Lung |
|
|
| Papillary Adenocarcinoma |
|
Infiltrating And Papillary Adenocarcinoma
|
Infiltrating Papillary Adenocarcinoma
|
|
Adenocarcinoma Papillary
|
Adenocarcinoma, Papillary
|
|
|
| Autosomal Recessive Congenital Ichthyosis |
|
Lamellar Ichthyosis
|
Congenital Ichthyosiform Erythroderma
|
|
Li
|
Congenital Nonbullous Ichthyosiform Erythroderma
|
|
Arci
|
Congenital Lamellar Ichthyosis
|
|
Nonbullous Congenital Ichthyosiform Erythroderma
|
Cie
|
|
Congenital Non-Bullous Ichthyosiform Erythroderma
|
Erythrodermic Ichthyosis
|
|
Nbcie
|
Ncie
|
|
Non-Bullous Congenital Ichthyosiform Erythroderma
|
Ichthyosis, Lamellar
|
|
Non Bullous Congenital Ichthyosiform Erythroderma
|
Ichthyosiform Erythroderma, Brocq Congenital, Nonbullous Form
|
|
Ichthyosiform Erythroderma, Congenital, Nonbullous, 1
|
Collodion Baby
|
|
Collodion Baby Syndrome
|
Ichthyoses, Lamellar
|
|
Nbie
|
Nonbullous Ichthyosiform Erythroderma
|
|
Classic Lamellar Ichthyosis
|
Ichthyosiform Erythroderma Nonbullous Congenital
|
|
Ichthyosiform Erythroderma Congenital
|
Ichthyosis, Congenital, Autosomal Recessive
|
|
Ichthyosiform Erythroderma, Congenital
|
Collodion Fetus
|
|
Non-Bullous Ichthyosiform Erythroderma
|
|
|
| Cystadenoma |
|
Cystoma
|
Craniopharyngioma
|
|
|
| Myoclonus |
|
|
| Body Mass Index Quantitative Trait Locus 11 |
|
OBESITY
|
Obesity, Susceptibility To
|
|
Leanness, Inherited
|
Obesity, Susceptibility To, Bmiq11
|
|
Obesity, Mild, Early-Onset
|
Obesity, Association With
|
|
Obesity, Early-Onset, Susceptibility To
|
Obesity, Severe
|
|
Obesity, Severe, And Type Ii Diabetes
|
Obesity, Late-Onset
|
|
BMIQ11
|
Obesity Bmiq11
|
|
Obesity, Early-Onset
|
Obesity , Susceptibility To
|
|
Simple Obesity Nos
|
Excess Fat
|
|
Obesity, Not Elsewhere Classified, Body Mass Index Not Elsewhere Classified
|
Adiposis
|
|
|
| Glucose Transporter Type 1 Deficiency Syndrome |
|
Glut1 Deficiency Syndrome
|
Encephalopathy Due To Glut1 Deficiency
|
|
De Vivo Disease
|
Glut1 Ds
|
|
G1d
|
Glucose Transport Defect, Blood-Brain Barrier
|
|
Glucose Transporter Protein Syndrome
|
Spastic Paraplegia-Epilepsy-Intellectual Disability Syndrome
|
|
Spemr
|
Glut-1 Deficiency Syndrome
|
|
Glut1 Deficiency
|
Gtps
|
|
Spastic Paraplegia, Epilepsy, And Mental Retardation
|
|
|
| Gastric Cancer |
|
Stomach Cancer
|
Stomach Carcinoma
|
|
Gastric Carcinoma
|
Gastric Cancer, Somatic
|
|
Gastric Neoplasm
|
Carcinoma Of Stomach
|
|
Stomach Neoplasms
|
Malignant Neoplasm Of Stomach
|
|
Gastric Cancer Risk After H. Pylori Infection
|
Cancer Of The Stomach
|
|
Adult Stomach Cancer
|
Adult Stomach Carcinoma
|
|
GASC
|
Gastric Cancer Intestinal
|
|
Gastric Cancers
|
Gastric Carcinomas
|
|
Cancer, Gastric
|
Stomach Neoplasm
|
|
Malignant Neoplasm Of Body Of Stomach
|
Malignant Tumor Of Lesser Curve Of Stomach
|
|
Gastrocarcinoma Of Unspecified Site
|
Leather Bottle Stomach
|
|
Carcinoma Of Fundus Of Stomach
|
Cancer Of Fundus Of Stomach
|
|
Primary Malignant Neoplasm Of Body Of Stomach
|
Cancer Of Body Of Stomach
|
|
Primary Malignant Neoplasm Of Pyloric Antrum
|
Pyloric Antrum Cancer
|
|
Malignant Tumour Of Stomach
|
|
|
| Acanthosis Nigricans |
|
|
| Hemiplegia |
|
Infantile Hemiplegia
|
Postnatal Infantile Hemiplegia
|
|
Hemiplegia, Infantile
|
|
|
| Pyruvate Dehydrogenase E1-Alpha Deficiency |
|
Pyruvate Dehydrogenase Deficiency
|
Pyruvate Dehydrogenase Complex Deficiency
|
|
Pyruvate Decarboxylase Deficiency
|
Pdh Deficiency
|
|
PDHAD
|
Pyruvate Dehydrogenase Complex Deficiency Disease
|
|
Ataxia With Lactic Acidosis I
|
Ataxia With Lactic Acidosis 1
|
|
Pdh
|
Pdhc
|
|
Ataxia With Lactic Acidosis
|
Ataxia, Intermittent, With Abnormal Pyruvate Metabolism
|
|
Ataxia, Intermittent, With Pyruvate Dehydrogenase Deficiency
|
Deficiency Of Pyruvic Dehydrogenase
|
|
Ataxia, Intermittent, With Pyruvate Dehydrogenase, Or Decarboxylase, Deficiency
|
Pdc Deficiency
|
|
Intermittent Ataxia With Pyruvate Dehydrogenase Deficiency
|
Pdhc Deficiency
|
|
Pyruvate Dehydrogenase Complex E1 Component Subunit Alpha Deficiency
|
Ataxia Intermittent With Abnormal Pyruvate Metabolism
|
|
Ataxia Intermittent With Pyruvate Dehydrogenase Or Decarboxylase Deficiency
|
Pyruvate Dehydrogenase E1 Alpha Deficiency
|
|
Pdc - [Pyruvate Dehydrogenase Complex] Deficiency
|
Ataxia With Lactic Acidosis 2
|
|
|
| Ichthyosis, Congenital, Autosomal Recessive 11 |
|
Autosomal Recessive Congenital Ichthyosis 11
|
Ichthyosis With Hypotrichosis, Autosomal Recessive
|
|
Arih
|
Ichthyosis And Follicular Atrophoderma With Hypotrichosis And Hypohidrosis
|
|
Autosomal Recessive Ichthyosis With Hypotrichosis
|
ARCI11
|
|
Ifah
|
Hypotrichosis-Congenital Ichthyosis Syndrome
|
|
Ichthyosis-Follicular Atrophoderma-Hypotrichosis Syndrome
|
Ichthyosis-Follicular Atrophoderma-Hypotrichosis-Hypohidrosis Syndrome
|
|
Ichthyosis-Hypotrichosis Syndrome
|
Ifah Syndrome
|
|
Ihs
|
|
|
| Episodic Ataxia, Type 8 |
|
Episodic Ataxia Type 8
|
EA8
|
|
Episodic Ataxia With Slurred Speech
|
|
|
| Paroxysmal Choreoathetosis |
|
Paroxysmal Nonkinesigenic Dyskinesia
|
|
|
| Epilepsy With Myoclonic Absences |
|
|
| Cardiovascular Organ Benign Neoplasm |
|
|
| 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
|
|
|
| Fetal Hemoglobin Quantitative Trait Locus 1 |
|
Hereditary Persistence Of Fetal Hemoglobin
|
Delta-Beta-Thalassemia
|
|
Delta-Beta Thalassemia
|
Delta Beta-Thalassemia
|
|
HBFQTL1
|
Hemoglobin F, Hereditary Persistence Of
|
|
Hpfh
|
Hereditary Persistence Of Fetal Hemoglobin, Hb Gene Cluster-Related
|
|
Hemoglobin, Fetal, Quantitative Trait Locus 1
|
Hereditary Persistence Of Fetal Hemoglobin Thalassemia
|
|
Hpfh - [Hereditary Persistence Of Fetal Haemoglobin]
|
Fetal Haemoglobin
|
|
Persistence Of Fetal Haemoglobin
|
Persistent Haemoglobin F
|
|
|
| Cryohydrocytosis |
|
CHC
|
Stomatocytosis, Cold-Sensitive
|
|
Hereditary Cryohydrocytosis With Normal Stomatin
|
Pseudohyperkalemia Cardiff
|
|
|
| Angiokeratoma Circumscriptum |
|
|
| Nervous System Disease |
|
Abnormality Of The Nervous System
|
Nervous System Diseases
|
|
Nervous System Disorder
|
|
|
| Paroxysmal Dystonia |
|
Paroxysmal Dyskinesia
|
Pxd - [Paroxysmal Dyskinesia]
|
|
|
| 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
|
|
|
| Mediastinum Sarcoma |
|
|
| Dravet Syndrome |
|
Severe Myoclonic Epilepsy Of Infancy
|
Smei
|
|
Severe Myoclonic Epilepsy In Infancy
|
Epileptic Encephalopathy, Early Infantile, 6
|
|
DRVT
|
Developmental And Epileptic Encephalopathy 6a
|
|
Dee6a
|
Eiee6
|
|
Dee6
|
Developmental And Epileptic Encephalopathy 6
|
|
Early Infantile Epileptic Encephalopathy 6
|
Myoclonic Epilepsy, Severe, Of Infancy
|
|
Sme
|
Severe Myoclonus Epilepsy Of Infancy
|
|
Borderline Smei
|
Smeb
|
|
Smeb-M
|
Smeb-O
|
|
Smeb-Sw
|
Smei-Borderland
|
|
Smei-Borderland More Than One Feature
|
Smei-Borderland-Myoclonic Seizures
|
|
Smei-Borderland-Spike Wave
|
Intractable Childhood Epilepsy With Generalized Tonic-Clonic Seizures
|
|
ICEGTC
|
Developmental And Epileptic Encephalopathy, 6
|
|
Infantile Severe Myoclonic Epilepsy
|
Epilepsy, Intractable Childhood, With Generalized Tonic-Clonic Seizures
|
|
|
| Deafness, Autosomal Recessive 2 |
|
DFNB2
|
Neurosensory Nonsyndromic Recessive Deafness 2
|
|
Nsrd2
|
Autosomal Recessive Nonsyndromic Deafness 2
|
|
Deafness, Autosomal Recessive, Type 2
|
Autosomal Recessive Deafness 2
|
|
Deafness, Autosomal Recessive, 2
|
Deafness Neurosensory Autosomal Recessive 2
|
|
Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 2
|
Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 2
|
|
Deafness, Autosomal Recessive 2, Neurosensory
|
|
|
| Ovarian Cancer |
|
Ovarian Carcinoma
|
Ovarian Neoplasm
|
|
Malignant Tumour Of Ovary
|
Epithelial Ovarian Cancer
|
|
Neoplasm Of Ovary
|
Ovarian Neoplasms
|
|
Ovarian Cancers
|
Malignant Neoplasm Of Ovary
|
|
Primary Malignant Neoplasm Of Ovary
|
Ovarian Cancer, Somatic
|
|
Malignant Ovarian Tumor
|
Ovary Neoplasm
|
|
Primary Ovarian Cancer
|
Tumor Of The Ovary
|
|
Cancer Of The Ovary
|
Malignant Neoplasm Of The Ovary
|
|
Malignant Tumor Of The Ovary
|
Ovarian Malignant Tumor
|
|
OC
|
Ovarian Carcinomas
|
|
Cancer, Ovarian
|
Cancer Of Ovary
|
|
Ovary Cancer
|
Ca Ovary
|
|
|
| Glut1 Deficiency Syndrome 2 |
|
Dystonia 18
|
Dyt18
|
|
Childhood Onset Glut1 Deficiency Syndrome 2
|
GLUT1DS2
|
|
Ped With Or Without Epilepsy And/Or Hemolytic Anemia
|
Paroxysmal Exertion-Induced Dyskinesia
|
|
Ped
|
Paroxysmal Exercise-Induced Dystonia
|
|
Paroxysmal Exercise-Induced Dyskinesia With Or Without Epilepsy And/Or Hemolytic Anemia
|
Paroxysmal Exertion-Induced Dystonia With Or Without Epilepsy And/Or Hemolytic Anemia
|
|
Glut1 Deficiency Syndrome 2, Childhood Onset
|
Dyt-Slc2a1
|
|
Dystonia-18
|
Paroxysmal Exercise-Induced Dystonia With Or Without Epilepsy And/Or Hemolytic Anemia
|
|
Paroxysmal Exertion-Induced Dyskinesia With Or Without Epilepsy And/Or Hemolytic Anemia
|
Glut1 Deficiency Syndrome, Type 2, Childhood Onset
|
|
|
| West Syndrome |
|
Infantile Spasms
|
Infantile Spasms Syndrome
|
|
Infantile Spasm
|
X-Linked Infantile Spasm Syndrome
|
|
X-Linked Infantile Spasms
|
Epileptic Encephalopathy, Early Infantile, 1
|
|
Is
|
Tonic Spasms With Clustering, Arrest Of Psychomotor Development And Hypsarrhythmia On Eeg
|
|
West'S Syndrome
|
Spasms, Infantile
|
|
Is -[Infantile Spasm]
|
Salaam Spasm
|
|
Salaam Tic
|
|
|
| Congenital Nervous System Abnormality |
|
Congenital Neurologic Anomaly
|
Congenital Nervous System Disorder
|
|
|
| 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
|
|
|
| Perineurioma |
|
|
| Hypopigmentation Of Eyelid |
|
|
| Endometrial Cancer |
|
Endometrial Carcinoma
|
Endometrial Neoplasm
|
|
Malignant Neoplasm Of Endometrium
|
Endometrioid Carcinoma
|
|
Endometrial Neoplasms
|
Carcinoma, Endometrioid
|
|
Endometrial Cancer, Familial
|
Endometrial Carcinoma, Somatic
|
|
Endometrial Cancer, Susceptibility To
|
Endometrial Ca
|
|
Malignant Endometrial Neoplasm
|
Neoplasm Of Endometrium
|
|
Primary Malignant Neoplasm Of Endometrium
|
Tumor Of Endometrium
|
|
Carcinoma Of The Endometrium
|
Endometrioid Carcinoma Of Female Reproductive System
|
|
ENDMC
|
Carcinoma Endometrioid
|
|
Endometrial Cancers
|
Cancer, Endometrial
|
|
Uterine Corpus Cancer
|
|
|
| Epilepsy, Idiopathic Generalized 12 |
|
EIG12
|
Epilepsy, Idiopathic Generalized, Susceptibility To, 12
|
|
Idiopathic Generalized Epilepsy 12
|
Susceptibility To Idiopathic Generalized Epilepsy 12
|
|
Epilepsy, Idiopathic, Generalized, Susceptibility To, Type 12
|
|
|
| Epilepsy |
|
Epilepsy Syndrome
|
Epileptic Syndrome
|
|
Epilepsies
|
Symptomatic Epilepsies
|
|
Post Traumatic Epilepsy
|
Traumatic Epilepsy
|
|
Traumatic Epileptic
|
Epilepsy Due To Hippocampal Sclerosis
|
|
Epilepsy With Ammon'S Horn Sclerosis
|
Epilepsy Due To Cortical Dysplasia
|
|
Epilepsy Due To Neuronal Migration Disorders
|
|
|
| Renal Pelvis Adenocarcinoma |
|
Adenocarcinoma Of Renal Pelvis
|
Adenocarcinoma Of The Kidney Pelvis
|
|
|
| Malignant Peripheral Nerve Sheath Tumor |
|
Mpnst
|
Malignant Neurilemmoma
|
|
Neurofibrosarcoma
|
Malignant Neurofibroma
|
|
Malignant Schwannoma
|
Neurogenic Sarcoma
|
|
Malignant Neoplasm Of The Peripheral Nerve Sheath
|
Schwannoma, Malignant
|
|
Malignant Peripheral Nerve Sheath Tumors
|
|
|
| Dehydrated Hereditary Stomatocytosis 1 With Or Without Pseudohyperkalemia And/Or Perinatal Edema |
|
Dehydrated Hereditary Stomatocytosis
|
Hereditary Xerocytosis
|
|
Xerocytosis, Hereditary
|
Pshk1
|
|
Pseudohyperkalemia Edinburgh
|
Dehydrated Hereditary Stomatocytosis With Or Without Pseudohyperkalemia And/Or Perinatal Edema
|
|
DHS1
|
Dhs
|
|
Hereditary Desiccytosis
|
Dehydrated Hereditary Stomatocytosis 1
|
|
Desiccytosis, Hereditary
|
Pseudohyperkalemia, Familial, 1, Due To Red Cell Leak
|
|
Pseudohyperkalemia Familial 1, Due To Red Cell Leak
|
Desiccytosis Hereditary
|
|
Xerocytosis Hereditary
|
Familial Pseudohyperkalemia 1 Due To Red Cell Leak
|
|
Stomatocytosis, Dehydrated, Hereditary, With/Without Pseudohyperkalemia And/Or Perinatal Edema
|
Xerocytosis
|
|
|
| Early Myoclonic Encephalopathy |
|
Myoclonic Epilepsy
|
Myoclonic Seizure
|
|
Epilepsies, Myoclonic
|
Epileptic Seizures - Myoclonic
|
|
Epileptic Seizures, Myoclonic
|
Myoclonia Epileptica
|
|
Myoclonic Seizure Disorder
|
Early Myoclonic Encephalopathy With Suppression-Bursts
|
|
|
| Hypoascorbemia |
|
Scurvy
|
Ascorbic Acid Deficiency
|
|
Vitamin C Deficiency
|
Vitamin C, Inability To Synthesize
|
|
Deficiency Of Vitamin C
|
Scorbutus
|
|
Vitamin C
|
|
|
| Diabetes Mellitus |
|
|
| Pyogenic Granuloma |
|
Lobular Capillary Hemangioma
|
Granuloma Pyogenic
|
|
Granuloma Pyogenicum
|
Granuloma Telangiectaticum Of Skin
|
|
Pyogenic Granuloma Of Skin
|
Lobular Capillary Haemangioma Of Skin
|
|
|
| Epilepsy, Idiopathic Generalized |
|
Idiopathic Generalized Epilepsy
|
Generalised Epilepsy
|
|
Epilepsy, Generalized
|
EIG
|
|
Ige
|
Epilepsy, Idiopathic Generalized, Susceptibility To, 1
|
|
Epilepsy, Idiopathic Generalized 1
|
Epilepsy, Idiopathic Generalized, Susceptibility To
|
|
Epilepsy, Idiopathic, Generalized
|
Epilepsy, Idiopathic, Generalized, Susceptibility To, Type 1
|
|
|
| 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
|
|
|
| Type 2 Diabetes Mellitus |
|
Insulin Resistance
|
NIDDM
|
|
Diabetes Mellitus, Non-Insulin-Dependent
|
Type 2 Diabetes
|
|
T2D
|
Noninsulin-Dependent Diabetes Mellitus
|
|
Diabetes Mellitus, Type Ii
|
Maturity-Onset Diabetes
|
|
Insulin Resistance, Severe, Digenic
|
Diabetes Mellitus, Type 2
|
|
Diabetes Mellitus, Noninsulin-Dependent
|
Diabetes Mellitus, Noninsulin-Dependent, Association With
|
|
Diabetes Mellitus, Noninsulin-Dependent, Late Onset
|
Hypertension, Insulin Resistance-Related, Susceptibility To
|
|
Insulin Resistance, Susceptibility To
|
Non-Insulin-Dependent Diabetes Mellitus
|
|
Type Ii Diabetes Mellitus
|
Adult-Onset Diabetes Mellitus
|
|
Maturity-Onset Diabetes Mellitus
|
Diabetes Mellitus Type 2
|
|
Type Ii Diabetes
|
Type 2 Diabetes Mellitus, Susceptibility To
|
|
Diabetes, Type 2
|
Diabetes Mellitus, Noninsulin-Dependent, Susceptibility To
|
|
Diabetes Mellitus, Non-Insulin-Dependent, Susceptibility To
|
Diabetes Mellitus, Type 2, Susceptibility To
|
|
Diabetes Mellitus, Noninsulin-Dependent, 2
|
Diabetes Mellitus, Type Ii, Susceptibility To
|
|
Hypertension, Insulin Resistance-Related
|
Adult-Onset Diabetes
|
|
Aodm
|
Diabetes Mellitus, Adult-Onset
|
|
Diabetes Mellitus Type Ii
|
Diabetes Mellitus Type 2, Susceptibility To
|
|
Diabetes, Type Ii, Susceptibility To
|
Diabetes Type 2
|
|
Diabetes Mellitus
|
Adult Onset Diabetes
|
|
Maturity Onset Diabetes
|
Nonketotic Diabetes
|
|
Non-Insulin Dependent Diabetes Mellitus
|
T2dm - [Type 2 Diabetes Mellitus]
|
|
Niddm - [Non Insulin Dependent Diabetes Mellitus]
|
Dm2
|
|
Dm Type Ii
|
Diabetic Type 2
|
|
Insulin Requiring Type 2 Diabetes
|
Noninsulin Dependent Diabetes
|
|
Non-Insulin-Dependent Diabetes Mellitus Without Complications
|
Diabetes Due To Insulin Secretory Defect
|
|
Diabetes Mellitus Due To Insulin Secretory Defect
|
Non-Insulin-Dependent Diabetes Of The Young
|
|
Senile Diabetes
|
Nonketotic Hyperglycaemia
|
|
Stable Diabetes
|
|
|
| Microcephaly |
|
Microencephaly
|
Microcephalus
|
|
Microcephalic
|
Nanocephaly
|
|
Congenital Microcephaly
|
Brain Hypoplasia
|
|
Brain Nondevelopment
|
Cephalic Hypoplasia
|
|
Undeveloped Cerebrum
|
Undeveloped Brain
|
|
Micrencephalon
|
Micrencephaly
|
|
|
| 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
|
|
|
| Peripheral Nervous System Disease |
|
Peripheral Neuropathy
|
Peripheral Nerve Disease
|
|
Peripheral Nerve Disorders
|
Neuropathy, Peripheral
|
|
Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation
|
|
|
| Renal Glucosuria |
|
Renal Glycosuria
|
Familial Renal Glucosuria
|
|
Glycosuria, Renal
|
GLYS
|
|
Glys1
|
Glucosuria, Renal
|
|
Renal Diabetes
|
Familial Renal Glycosuria
|
|
Sglt2 Deficiency
|
Gly
|
|
Diabetes Renal
|
|
|
| Epilepsy, Pyridoxine-Dependent |
|
Pyridoxine-Dependent Epilepsy
|
PDE
|
|
Pyridoxine Dependency With Seizures
|
Vitamin B6-Dependent Seizures
|
|
EPD
|
Aasa Dehydrogenase Deficiency
|
|
Antiquitin Deficiency
|
Pyridoxine Dependency
|
|
Glutamate Decarboxylase Deficiency
|
Pyridoxine-Dependent Seizures
|
|
Deficiency Of Glutamate Decarboxylase
|
|
|
| Capillary Disease |
|
|
| Maturity-Onset Diabetes Of The Young |
|
MODY
|
Maturity Onset Diabetes Mellitus In Young
|
|
Mason-Type Diabetes
|
Mason Type Diabetes
|
|
Maturity Onset Diabetes Of The Young
|
Mody Syndrome
|
|
Diabetes Of The Young, Maturity-Onset
|
|
|
| Hypoglycemia |
|
Hypoglycaemia
|
Low Blood Sugar
|
|
Hypoglycaemia Nos
|
Spontaneous Hypoglycaemia
|
|
Nondiabetic Hypoglycaemia
|
Hypoglycaemic Disorder Nos
|
|
Hypoglycaemic Syndrome
|
|
|
| Necrobiosis Lipoidica |
|
Oppenheim-Urbach Disease
|
Necrobiosis Lipoidica Diabeticorum
|
|
|
| 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
|
|
|
| Stomatin-Deficient Cryohydrocytosis With Neurologic Defects |
|
Hereditary Cryohydrocytosis With Reduced Stomatin
|
SDCHCN
|
|
Glut1 Deficiency Syndrome With Pseudohyperkalemia And Hemolysis
|
Cryohydrocytosis, Stomatin-Deficient, With Mental Retardation, Seizures, Cataracts, And Massive Hepatosplenomegaly
|
|
Chc Type 2
|
Hereditary Cryohydrocytosis Type 2
|
|
Stomatin-Deficient Cryohydrocytosis
|
Sdchc
|
|
Cryohydrocytosis, Stomatin-Deficient, With Neurologic Defects
|
|
|
| Benign Familial Infantile Epilepsy |
|
Benign Familial Infantile Seizures
|
Bfie
|
|
Benign Familial Infantile Convulsion
|
Bfic
|
|
Bfis
|
Benign Familial Infantile Convulsions
|
|
Familial Benign Neonatal Epilepsy
|
Watanabe-Vigevano Syndrome
|
|
|
| Fat Necrosis Of Breast |
|
Breast Fat Necrosis
|
Aseptic Fat Necrosis Of Breast
|
|
Breast Necrosis Nos
|
|
|
| Early Onset Absence Epilepsy |
|
|
| Skin Hemangioma |
|
Angioma Of The Skin
|
Angiomatous Naevus Of Skin
|
|
Hemangioma Of Skin
|
|
|
| Movement Disease |
|
Movement Disorders
|
Movement Disorder
|
|
|
| Migraine With Aura |
|
Classic Migraine
|
Migraine With Typical Aura
|
|
Migraine Accompagnée
|
Complicated Migraine
|
|
Classical Migraine
|
Acute Migraine With Aura
|
|
|
| Spasticity |
|
|
| Hyperglycemia |
|
|
| 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
|
|
|
| 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
|
|
|
| Capillary Hemangioma |
|
Strawberry Nevus Of Skin
|
Cellular Hemangioma Of Infancy
|
|
Congenital Vascular Hamartoma
|
Congenital Vascular Naevus
|
|
Infantile Hemangioma
|
Juvenile Hemangioma
|
|
Strawberry Haemangioma
|
Strawberry Nevus
|
|
Hemangioma Capillary
|
Hemangioma, Capillary
|
|
Hemangioma, Cavernous
|
|
|
| Pacinian Tumor |
|
|
| Choreatic Disease |
|
|
| Arteriovenous Malformation |
|
Arteriovenous Malformations
|
Arteriovenous Hemangioma
|
|
Cirsoid Aneurysm
|
Racemose Aneurysm
|
|
Racemose Angioma
|
Racemose Hemangioma
|
|
Congenital Arteriovenous Malformation
|
|
|
| Dystonia, Dopa-Responsive |
|
Dystonia 5
|
Dopa-Responsive Dystonia
|
|
DRD
|
Dyt5
|
|
Dystonia-Parkinsonism With Diurnal Fluctuation
|
Dyt-Th
|
|
Hpd With Diurnal Fluctuation
|
Hereditary Progressive Dystonia With Diurnal Fluctuation
|
|
Dystonia, Progressive, With Diurnal Variation
|
Segawa Syndrome, Autosomal Dominant
|
|
Dystonia, Dopa-Responsive, Autosomal Dominant
|
Dopa-Responsive Dystonia, Autosomal Dominant
|
|
Dystonia, Dopa-Responsive, With Or Without Hyperphenylalaninemia
|
Dyt-Gch1
|
|
Dyt-Spr
|
Dystonia 5, Dopa-Responsive Type
|
|
Hereditary Progressive Dystonia With Marked Diurnal Fluctuation
|
Autosomal Dominant Dopa-Responsive Dystonia
|
|
Autosomal Dominant Segawa Syndrome
|
Dystonia-5
|
|
Progressive Dystonia With Diurnal Fluctuation
|
Dystonia, Type 5, Dopa-Responsive Type
|
|
|
| Glycine Encephalopathy |
|
Non-Ketotic Hyperglycinemia
|
Nonketotic Hyperglycinemia
|
|
NKH
|
GCE
|
|
Hyperglycinemia, Nonketotic
|
Hyperglycinemia Nonketotic
|
|
Infantile Glycine Encephalopathy
|
Encephalopathy, Glycine
|
|
Glycine Synthase Deficiency
|
Nka
|
|
Neonatal Glycine Encephalopathy
|
Classic Glycine Encephalopathy
|
|
Neonatal Nkh
|
Neonatal Non-Ketotic Hyperglycinemia
|
|
Infantile Nkh
|
Infantile Non-Ketotic Hyperglycinemia
|
|
Non-Ketotic Hyperglycinaemia
|
Glycine Cleavage Deficiency
|
|
Nonketotic Hyperglycinaemia
|
|
|
| Tuberous Sclerosis |
|
Tuberous Sclerosis Syndrome
|
Bourneville'S Disease
|
|
Epiloia
|
Cerebral Sclerosis
|
|
Tuberose Sclerosis
|
Tuberous Sclerosis 1
|
|
Bourneville Disease
|
Bourneville Phakomatosis
|
|
Pringle'S Disease
|
|
|
| Angiokeratoma |
|
Angiokeratoma Of Skin
|
Cutaneous Angiokeratoma
|
|
Skin Angiokeratoma
|
|
|
| Strabismus |
|
Strabismus, Susceptibility To
|
Strabismus, Susceptibility To, 1
|
|
Strabismus 1
|
|
|
| Glut1 Deficiency Syndrome 1 |
|
GLUT1DS1
|
Glucose Transport Defect, Blood-Brain Barrier
|
|
Encephalopathy Due To Glut1 Deficiency
|
Glut1 Deficiency Syndrome 1, Infantile Onset, Severe
|
|
Classic Glucose Transporter Type 1 Deficiency Syndrome
|
Classic Glut1 Deficiency Syndrome
|
|
Classic Glut1-Ds
|
De Vivo Disease
|
|
Blood-Brain Barrier Glucose Transport Defect
|
Glut1 Deficiency
|
|
Glut-1 Deficiency Syndrome
|
Glut1 Deficiency Syndrome Autosomal Recessive
|
|
Glut1 Deficiency Syndrome, Type 1, Infantile Onset, Severe
|
Glut1 Deficiency Syndrome
|
|
|
| Metagonimiasis |
|
Trematode Infections
|
Infection By Metagonimus Yokogawai
|
|
Metagonimus Yokogawai Infection
|
|
|
| Early Infantile Epileptic Encephalopathy |
|
Early Infantile Epileptic Encephalopathy With Suppression Bursts
|
Early Infantile Epileptic Encephalopathy With Burst-Suppression
|
|
Eiee
|
Early Infantile Epileptic Encephalopathy With Suppression-Bursts
|
|
Ohtahara Syndrome
|
Encephalopathy, Epileptic, Early Infantile
|
|
|
| Gestational Diabetes |
|
Gestational Diabetes Mellitus
|
GDM
|
|
Diabetes Mellitus Arising In Pregnancy
|
Maternal Gestational Diabetes Mellitus
|
|
Diabetes Mellitus, Gestational
|
Diabetes Mellitus, Pregnancy Related
|
|
Diabetes, Pregnancy-Induced
|
Diabetes Gestational
|
|
Diabetes, Gestational
|
Diabetes Of Pregnancy
|
|
Gdm - [Gestational Diabetes Mellitus]
|
Gestational Diabetes Mellitus Nos
|
|
Gestational Diabetes Complicating Pregnancy, Childbirth, Or The Puerperium
|
|
|
| Epilepsy With Myoclonic-Atonic Seizures |
|
Doose Syndrome
|
Epilepsy With Myoclonic-Astatic Seizures
|
|
Myoclonic Astatic Epilepsy
|
Epilepsy With Myoclono-Astatic Crisis
|
|
Myoclonic-Astatic Epilepsy
|
Emas
|
|
Mae
|
Myoclonic Atonic Epilepsy
|
|
Myoclonic-Astatic Epilepsy In Early Childhood
|
|
|
| Developmental And Epileptic Encephalopathy |
|
Encephalopathy, Developmental And Epileptic
|
|
|
| Intraneural Perineurioma |
|
|
| Childhood Electroclinical Syndrome |
|
|
| Benign Epilepsy With Centrotemporal Spikes |
|
Benign Rolandic Epilepsy
|
Rolandic Epilepsy
|
|
Epilepsy, Rolandic
|
Bcects
|
|
Benign Childhood Epilepsy With Centrotemporal Spike
|
Sylvan Seizures
|
|
Becrs
|
Bects
|
|
Bre
|
Benign Epilepsy Of Childhood With Centrotemporal Spikes
|
|
Benign Familial Epilepsy Of Childhood With Rolandic Spikes
|
Centrotemporal Epilepsy
|
|
|
| Cavernous Hemangioma |
|
Hemangioma, Cavernous
|
Cavernoma
|
|
Cavernous Haemangioma
|
|
|
| Lennox-Gastaut Syndrome |
|
Epileptic Encephalopathy Lennox-Gastaut Type
|
Lennox Syndrome
|
|
Encephalopathy Of Childhood
|
Childhood Epileptic Encephalopathy With Diffuse Slow Spikes And Waves
|
|
Lgs
|
|
|
| T-Cell Acute Lymphoblastic Leukemia |
|
T-Cell Leukemia
|
Acute T Cell Leukemia
|
|
Precursor T Lymphoblastic Leukemia
|
Precursor T-Lymphoblastic Lymphoma/Leukemia
|
|
T Acute Lymphoblastic Leukemia
|
T-Cell Acute Lymphocytic Leukaemia
|
|
T-Cell Lymphoblastic Leukemia/Lymphoma
|
Leukemia T-Cell
|
|
Leukemia, T-Cell
|
Leukemia, Acute, Lymphoblastic, T-Cell
|
|
Leukemia, T-Cell Acute Lymphoblastic
|
Leukemia, Acute T-Cell
|
|
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
|
Precursor T-Cell Lymphoblastic Lymphoma
|
|
Precursor T Cell Lymphoblastic Leukemia/Lymphoblastic Lymphoma
|
|
|
| Childhood Absence Epilepsy |
|
Pyknolepsy
|
Petit Mal Epilepsy
|
|
Absence Seizures
|
Absence Seizure
|
|
Petit Mal Seizure
|
Absence Epilepsy, Childhood
|
|
Pykno-Epilepsy
|
Epilepsy, Absence
|
|
Absence Epilepsy
|
Pycnolepsy
|
|
|
| Aceruloplasminemia |
|
Cerebellar Ataxia
|
Hypoceruloplasminemia
|
|
Hemosiderosis, Systemic, Due To Aceruloplasminemia
|
Familial Apoceruloplasmin Deficiency
|
|
Hereditary Ceruloplasmin Deficiency
|
Deficiency Of Ferroxidase
|
|
Hypoceruloplasminemia, Hereditary
|
Ceruloplasmin Deficiency
|
|
Systemic Hemosiderosis Due To Aceruloplasminemia
|
ACERULOP
|
|
|
