| Diseases |
Alias |
|
| Hyperaldosteronism, Familial, Type Ii |
|
Familial Hyperaldosteronism Type Ii
|
Familial Hyperaldosteronism Type 2
|
|
HALD2
|
Fh Ii
|
|
Fh2
|
Familial Adrenal Adenoma
|
|
Fh-Ii
|
Fhii
|
|
Hyperaldosteronism Familial Type 2
|
Hyperaldosteronism, Familial, 2
|
|
|
| Leukoencephalopathy With Ataxia |
|
|
| Epilepsy, Idiopathic Generalized 11 |
|
Epilepsy, Idiopathic Generalized, Susceptibility To, 11
|
EIG11
|
|
Epilepsy, Juvenile Absence 2
|
Epilepsy, Juvenile Myoclonic 8
|
|
Idiopathic Generalized Epilepsy 11
|
Epilepsy, Juvenile Absence, Susceptibility To, 2
|
|
Epilepsy, Juvenile Myoclonic, Susceptibility To, 8
|
Susceptibility To Idiopathic Generalized Epilepsy 11
|
|
Juvenile Absence Epilepsy 2
|
JAE2
|
|
Eja2
|
Susceptibility To Juvenile Absence Epilepsy 2
|
|
Juvenile Myoclonic Epilepsy 8
|
EJM8
|
|
Susceptibility To Juvenile Myoclonic Epilepsy 8
|
Epilepsy, Idiopathic, Generalized, Susceptibility To, Type 11
|
|
|
| Clcn2-Related Leukoencephalopathy |
|
Leukoencephalopathy With Mild Cerebellar Ataxia And White Matter Edema
|
Leukoencephalopathy With Ataxia
|
|
Cc2l
|
Leukoencephalopathy With White Matter Edema
|
|
Lkpat
|
|
|
| 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]
|
|
|
| Juvenile Absence Epilepsy |
|
Epilepsy Juvenile Absence
|
Jae
|
|
Childhood Absence Epilepsy
|
Absence Epilepsy
|
|
|
| Constipation |
|
|
| Megalencephalic Leukoencephalopathy With Subcortical Cysts |
|
Vacuolating Megalencephalic Leukoencephalopathy With Subcortical Cysts
|
Mlc
|
|
Van Der Knaap Disease
|
Lvm
|
|
Leukoencephalopathy With Swelling And Cysts
|
Megalencephaly-Cystic Leukodystrophy
|
|
Megalencephalic Leukodystrophy Megalencephaly-Cystic Leukodystorphy Syndrome
|
Infantile Leukoencephalopathy And Megalencephaly
|
|
Leukoencephalopathy With Swelling And A Discrepantly Mild Course
|
Vacuolating Leukoencephalopathy
|
|
Megalencephalic Leukodystrophy
|
Megalencephaly-Cystic Leukodystrophy Syndrome
|
|
Van Der Knaap Syndrome
|
Leukoencephalopathy, Megalencephalic, With Subcortical Cysts
|
|
|
| Cerebral Palsy |
|
Infantile Cerebral Palsy
|
Mixed Cerebral Palsy
|
|
Palsy Cerebral
|
Palsy, Cerebral
|
|
Cerebral Palsy, Mixed
|
|
|
| Anismus |
|
|
| 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
|
|
|
| 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
|
|
|
| Enterocele |
|
Vaginal Enterocele
|
Hernia
|
|
Hernias
|
|
|
| Cystic Fibrosis |
|
Mucoviscidosis
|
CF
|
|
Pseudomonas Aeruginosa, Susceptibility To Chronic Infection By, In Cystic Fibrosis
|
Pseudomonas Aeruginosa Chronic Infection By, In Cystic Fibrosis
|
|
Cystic Fibrosis Lung Disease, Modifier Of
|
Cystic Fibrosis Of Pancreas
|
|
Fibrocystic Disease Of Pancreas
|
Cf - [Cystic Fibrosis]
|
|
Cystic Fibrosis Nos
|
Fibrocystic Disease
|
|
Fibrocystic Disease Of The Pancreas
|
Mucoviscidosis Of Pancreas
|
|
Nonproliferative Fibrocystic Disease
|
Pancreatic Cystic Fibrosis
|
|
|
| Prolapse Of Female Genital Organ |
|
|
| Hypokalemia |
|
Potassium Deficiency
|
Potassium Deficiency Disorder
|
|
Hypopotassemia
|
Potassium
|
|
Potassium [K] Deficiency
|
Hypokalaemic Syndrome
|
|
Hypopotassaemia
|
Hypopotassaemia Syndrome
|
|
Hypokalaemic
|
Potassium Depletion
|
|
|
| Cerebral Arteriopathy, Autosomal Dominant, With Subcortical Infarcts And Leukoencephalopathy, Type 2 |
|
CADASIL2
|
Cadasil 2
|
|
Autosomal Dominant Cerebral Arteriopathy With Subcortical Infarcts And Leukoencephalopathy Type 2
|
Htra1-Related Autosomal Dominant Cerebral Small Vessel Disease
|
|
Htra1-Related Autosomal Dominant Cerebral Angiopathy
|
Cerebral Arteriopathy, Autosomal Dominant, With Subcortical Infarcts And Leukoencephalopathy, 2
|
|
Cerebral Arteriopathy With Subcortical Infarcts And Leukoencephalopathy, Autosomal Dominant, 2
|
|
|
| Adolescence-Adult Electroclinical Syndrome |
|
|
| Anal Spasm |
|
Proctospasm
|
Anorectal Spasm
|
|
Rectal Spasm
|
|
|
| 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
|
|
Cushing'S Disease
|
Adrenal Cortex Adenoma
|
|
Corticotroph Pituitary Adenoma
|
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
|
|
|
| Osteochondrosis |
|
Osteochondritis
|
Apophysitis
|
|
Epiphysitis
|
Osteochondritis Juvenilis
|
|
Epiphyseal Necrosis
|
Juvenile Osteochondrosis Of Tibial Tubercle
|
|
|
| Functional Diarrhea |
|
|
| Hyperaldosteronism, Familial, Type I |
|
Glucocorticoid-Remediable Aldosteronism
|
Gra
|
|
Familial Hyperaldosteronism Type 1
|
Hyperaldosteronism, Familial Type 1
|
|
HALD1
|
Fh I
|
|
Glucocorticoid-Suppressible Hyperaldosteronism
|
Gsh
|
|
Acth-Dependent Hyperaldosteronism Syndrome
|
Aldosteronism, Glucocorticoid-Remediable
|
|
Dexamethasone Sensitive Hypertension
|
Glucocorticoid Sensitive Hypertension
|
|
Familial Hyperaldosteronism Type I
|
Fh1
|
|
Aldosteronism, Sensitive To Dexamethasone
|
Dexamethasone-Sensitive Hypertension
|
|
Fh-I
|
Glucocorticoid-Sensitive Hypertension
|
|
Hyperaldosteronism, Familial, 1
|
Aldosteronism Sensitive To Dexamethasone
|
|
Familial Hyperaldosteronism 1
|
Fh Type 1
|
|
Familial Aldosteronism Type I
|
|
|
| Hypothalamic Neoplasm |
|
Hypothalamic Neoplasms
|
Neoplasm Of The Hypothalamus
|
|
Tumor Of Hypothalamus
|
|
|
| Diencephalic Neoplasm |
|
Malignant Diencephalic Neoplasm
|
Malignant Diencephalic Tumor
|
|
Tumor Of Diencephalon
|
|
|
| Cerebral Arteriopathy, Autosomal Dominant, With Subcortical Infarcts And Leukoencephalopathy, Type 1 |
|
Cadasil
|
Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts And Leukoencephalopathy
|
|
Casil
|
Cerebral Arteriopathy With Subcortical Infarcts And Leukoencephalopathy
|
|
Familial Vascular Leukoencephalopathy
|
CADASIL1
|
|
Cadasil 1
|
Hereditary Multi-Infarct Dementia
|
|
Cadasil Syndrome
|
Dementia, Hereditary Multiinfarct Type
|
|
Cerebral Arteriopathy With Subcortical Infarcts And Leukoencephalopathy 1
|
Autosomal Dominant Cerebral Arteriopathy With Subcortical Infarcts And Leukoencephalopathy Type 1
|
|
Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts Leukoencephalopathy
|
Dementia, Hereditary Multi-Infarct Type
|
|
Hereditary Dementia, Multi-Infarct Type
|
Cerebral Autosomal Dominant Arteriopathy-Subcortical Infarcts-Leukoencephalopathy
|
|
Cerebral Arteriopathy, Autosomal Dominant, With Subcortical Infarcts And Leukoencephalopathy, 1
|
Cerebral Arteriopathy With Subcortical Infarcts And Leukoencephalopathy, Autosomal Dominant
|
|
Dementia Hereditary Multiinfarct Type
|
Dementia Hereditary Multi-Infarct Type
|
|
Arteriopathy, Cerebral, Autosomal Dominant, With Subcortical Infarcts And Leukoencephalopathy
|
|
|
| Myotonia Congenita |
|
Congenital Myotonia, Autosomal Dominant Form
|
Congenital Myotonia
|
|
Thomsen And Becker Disease
|
Thomsen Disease
|
|
Thomsen'S Disease
|
Generalized Myotonia Of Thomsen
|
|
Congenital Myotonic Muscular Dystrophy
|
Myotonia Congenita Nos
|
|
|
| Primary Pigmented Nodular Adrenocortical Disease |
|
Ppnad
|
Primary Pigmented Nodular Adrenal Dysplasia
|
|
Pigmented Nodular Adrenocortical Disease, Primary, 2
|
Pigmented Nodular Adrenocortical Disease, Primary, 1
|
|
|
| Childhood Absence Epilepsy |
|
Pyknolepsy
|
Petit Mal Epilepsy
|
|
Absence Seizures
|
Absence Seizure
|
|
Petit Mal Seizure
|
Absence Epilepsy, Childhood
|
|
Pykno-Epilepsy
|
Epilepsy, Absence
|
|
Absence Epilepsy
|
Pycnolepsy
|
|
|
| Autosomal Dominant Nocturnal Frontal Lobe Epilepsy |
|
Adnfle
|
Autosomal Dominant Sleep-Related Hypermotor Epilepsy
|
|
Enfl
|
Benign Familial Infantile Seizures 6
|
|
Benign Familial Infantile Seizures, 6
|
Nocturnal Frontal Lobe Epilepsy-4
|
|
Enfl1
|
Epilepsy, Nocturnal Frontal Lobe, 1
|
|
Epilepsy, Nocturnal Frontal Lobe, Type 1
|
|
|
| Generalized Epilepsy With Febrile Seizures Plus |
|
Gefs+
|
Genetic Epilepsy With Febrile Seizures Plus
|
|
Generalized Epilepsy With Febrile Seizures-Plus
|
Genetic Epilepsy With Febrile Seizures-Plus
|
|
Epilepsy, Generalized, With Febrile Seizures Plus
|
|
|
| Leukoencephalopathy With Vanishing White Matter |
|
Cree Leukoencephalopathy
|
Vanishing White Matter Disease
|
|
Ovarioleukodystrophy
|
Vanishing White Matter Leukodystrophy
|
|
Childhood Ataxia With Central Nervous System Hypomyelinization
|
Cach
|
|
Cach Syndrome
|
Myelinosis Centralis Diffusa
|
|
VWM
|
Cle
|
|
Childhood Ataxia With Central Nervous System Hypomyelination
|
Childhood Ataxia With Diffuse Central Nervous System Hypomyelination
|
|
Cach/Vwm
|
Cach/Vwm Syndrome
|
|
Childhood Ataxia With Central Nervous System Hypomyelination/Vanishing White Matter
|
Cree Leukoencehalopathy
|
|
Late Infantile Cach Syndrome
|
Juvenile Or Adult Cach Syndrome
|
|
Congenital Or Early Infantile Cach Syndrome
|
Leukodystrophy With Vanishing White Matter
|
|
|
| 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
|
|
|
| Benign Epilepsy With Centrotemporal Spikes |
|
Rolandic Epilepsy
|
Benign 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
|
|
|
| Developmental And Epileptic Encephalopathy |
|
Encephalopathy, Developmental And Epileptic
|
|
|
