| Diseases |
Alias |
|
| Migraine, Familial Hemiplegic, 2 |
|
FHM2
|
Mhp2
|
|
Migraine, Familial Basilar
|
Familial Hemiplegic Migraine 2
|
|
Familial Hemiplegic Migraine-2
|
Familiar Basilar Migraine
|
|
Migraine, Hemiplegic, Familial, Type 2
|
|
|
| Alternating Hemiplegia Of Childhood 1 |
|
AHC1
|
Hemiplegia, Alternating, Of Childhood, Type 1
|
|
|
| Developmental And Epileptic Encephalopathy 98 |
|
|
| Fetal Akinesia, Respiratory Insufficiency, Microcephaly, Polymicrogyria, And Dysmorphic Facies |
|
|
| Familial Hemiplegic Migraine |
|
Hemiplegic Migraine, Familial
|
Hemiplegic-Ophthalmoplegic Migraine
|
|
Fhm
|
Hemiplegic Migraine Familial
|
|
|
| Polymicrogyria |
|
|
| Alternating Hemiplegia Of Childhood |
|
Alternating Hemiplegia
|
Ahc
|
|
Alternating Hemiplegia Syndrome
|
Hemiplegia, Alternating, Of Childhood
|
|
Hemiplegia, Crossed
|
|
|
| Familial Or Sporadic Hemiplegic Migraine |
|
|
| Non-Specific Early-Onset Epileptic Encephalopathy |
|
Undetermined Early-Onset Epileptic Encephalopathy
|
Non-Specific Eoee
|
|
Undetermined Eoee
|
|
|
| Spastic Ataxia |
|
|
| Hemiplegia |
|
Infantile Hemiplegia
|
Postnatal Infantile Hemiplegia
|
|
Hemiplegia, Infantile
|
|
|
| Migraine With Aura |
|
Classic Migraine
|
Migraine With Typical Aura
|
|
Migraine Accompagnée
|
Complicated Migraine
|
|
Classical Migraine
|
Acute Migraine With Aura
|
|
|
| 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
|
|
|
| Migraine With Brainstem Aura |
|
Basilar Migraine
|
Basilar-Type Migraine
|
|
Basilar Artery Migraine
|
Bickerstaff Migraine
|
|
Brainstem Migraine
|
Mba
|
|
Vertebrobasilar Migraine
|
Basilar Artery Migraines
|
|
|
| Migraine Without Aura |
|
Common Migraine
|
Migraine With Or Without Aura, Susceptibility To
|
|
Migraine Without Aura, Susceptibility To
|
Acute Migraine Without Aura
|
|
|
| Neuronal Migration Disorders |
|
Abnormality Of Neuronal Migration
|
Malformations Of Cortical Development, Group Ii
|
|
Neuronal Dysmigration Syndromes
|
|
|
| Migraine, Familial Hemiplegic, 3 |
|
FHM3
|
Familial Hemiplegic Migraine 3
|
|
Mhp3
|
Migraine, Hemiplegic, Familial, Type 3
|
|
|
| Hydrops Fetalis, Nonimmune |
|
Hydrops Fetalis
|
Non-Immune Hydrops Fetalis
|
|
NIHF
|
Familial Non-Immune Hydrops Fetalis
|
|
Hydrops Fetalis Nonimmune
|
Idiopathic Hydrops Fetalis
|
|
Hb Bart'S Hydrops Fetalis
|
Alpha-Thalassemia Hydrops Fetalis
|
|
Alpha-Thalassemia Major
|
Hemoglobin Bart'S Hydrops Fetalis
|
|
Homozygous Alpha0-Thalassemia
|
Fetal Anasarca
|
|
Fetal Hydrops
|
Generalized Fetal Edema
|
|
Hf
|
Non-Immune Hf
|
|
Non-Immune Fetal Edema
|
Non-Immune Fetal Hydrops
|
|
Hydrops Fetalis, Non-Immune
|
Hemoglobin Bart'S Hydrops Syndrome
|
|
|
| Migraine, Familial Hemiplegic, 1 |
|
FHM1
|
Mhp1
|
|
Fhm
|
Familial Hemiplegic Migraine 1
|
|
Migraine, Familial Hemiplegic, 1, With Progressive Cerebellar Ataxia
|
Familial Hemiplegic Migraine1 With Progressive Cerebellar Ataxia
|
|
Migraine Familial Hemiplegic With Progressive Cerebellar Ataxia
|
Migraine, Hemiplegic, Familial, Type 1
|
|
Hemiplegic Migraine, Familial Type 1
|
|
|
| Distal Arthrogryposis |
|
Arthrogryposis Multiplex Congenita
|
Arthrogryposis
|
|
Congenital Multiple Arthrogryposis
|
Congenital Arthromyodysplasia
|
|
Fibrous Ankylosis Of Multiple Joints
|
Guerin-Stern Syndrome
|
|
Guérin-Stern Syndrome
|
Myodystrophia Fetalis Deformans
|
|
Otto Syndrome
|
Rocher-Sheldon Syndrome
|
|
Rossi Syndrome
|
Amc
|
|
Multiple Congenital Arthrogryposis
|
Arthrogryposis Syndrome
|
|
Arthrogryposis, Distal
|
Distal Arthrogryposis Syndrome
|
|
Freeman-Sheldon Syndrome
|
Arthrogryposis, Distal, Type 2b
|
|
Congenital Multiplex Arthrogryposis
|
Amyoplasia Congenita
|
|
Congenital Amyoplasia
|
Amc - [Arthrogryposis Multiplex Congenita]
|
|
|
| Migraine With Or Without Aura 1 |
|
Migraine
|
Migraine With Or Without Aura, Susceptibility To, 1
|
|
Migraine Disorder
|
Migraine Variant
|
|
Migraines
|
Migraine Disorders
|
|
Mgr1
|
Mgau
|
|
Ma
|
Migraine With Or Without Aura
|
|
Classic Migraine
|
Common Migraine
|
|
Disorder, Migraine
|
Headache Migraine
|
|
Headache Migrainous
|
Migraine Headache
|
|
Migraine Syndrome
|
Headache Including Migraine
|
|
Migraine, Susceptibility To
|
|
|
| Quadriplegia |
|
|
| Episodic Ataxia, Type 5 |
|
Episodic Ataxia Type 5
|
EA5
|
|
Episodic Ataxia 5
|
Ea-5
|
|
Ataxia, Episodic, Type 5
|
|
|
| Headache |
|
|
| Spinocerebellar Ataxia 6 |
|
Spinocerebellar Ataxia Type 6
|
SCA6
|
|
Type 6 Spinocerebellar Ataxia
|
Spinocerebellar Ataxia-6
|
|
Ataxia, Spinocerebellar, Type 6
|
|
|
| Episodic Ataxia, Type 2 |
|
Episodic Ataxia Type 2
|
EA2
|
|
Apca
|
Capa
|
|
Cerebellopathy, Hereditary Paroxysmal
|
Acetazolamide-Responsive Hereditary Paroxysmal Cerebellar Ataxia
|
|
Cerebellar Ataxia, Paroxysmal, Acetazolamide-Responsive
|
Episodic Ataxia With Nystagmus
|
|
Ataxia, Episodic, With Nystagmus
|
Episodic Ataxia, Nystagmus-Associated
|
|
Ataxia, Familial Paroxysmal
|
Acetazolamide-Responsive Episodic Ataxia Syndrome
|
|
Acetazolamide-Responsive, Hereditary, Paroxysmal, Cerebellar Ataxia
|
Ataxia, Familial, Paroxysmal
|
|
Nystagmus-Associated Episodic Ataxia
|
Familial Paroxysmal Ataxia
|
|
Episodic Ataxia 2
|
Ea-2
|
|
Episodic Ataxia Nystagmus-Associated
|
Hereditary Paroxysmal Cerebellopathy
|
|
Ataxia, Episodic, Type 2
|
|
|
| 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
|
|
|
| Hypomagnesemia 2, Renal |
|
Renal Hypomagnesemia 2
|
HOMG2
|
|
Magnesium Wasting, Renal
|
Autosomal Dominant Primary Hypomagnesemia With Hypocalciuria
|
|
Magnesium Loss, Isolated Renal
|
Isolated Autosomal Dominant Hypomagnesemia
|
|
Isolated Renal Magnesium Wasting
|
Renal Hypomagnesemia Type 2
|
|
Hypomagnesemia 2
|
Dominant Renal Hypomagnesemia
|
|
Hypomagnesemia With Hypocalciuria
|
Isolated Renal Magnesium Loss
|
|
Renal Magnesium Wasting
|
Hypomagnesemia-2, Renal
|
|
Renal Hypomagnesemia, Dominant
|
Hypomagnesemia, Type 2, Renal
|
|
|
| Episodic Ataxia |
|
Isaacs Syndrome
|
Neuromyotonia
|
|
Isaacs' Syndrome
|
Acquired Neuromyotonia
|
|
Continuous Muscle Fiber Activity Syndrome
|
Quantal Squander Syndrome
|
|
Isaacs-Mertens Syndrome
|
Ea Syndrome
|
|
Episodic Ataxia Syndrome
|
Isaac Syndrome
|
|
Isaac'S-Merten'S Syndrome
|
Isaac-Mertens Syndrome
|
|
Peripheral Nerve Hyperexcitability
|
Ea
|
|
Peripheral Nerve Hyperexcitability Syndrome
|
Ataxia, Episodic
|
|
Isaacs Neuromyotonia
|
Continuous Muscle Fibre Activity
|
|
|
| Dystonia 12 |
|
DYT12
|
Rdp
|
|
Generalized Dystonia
|
Dystonia-12
|
|
Rapid-Onset Dystonia-Parkinsonism
|
Familial Dystonia
|
|
Dystonia Musculorum Deformans
|
Dystonic Disorders
|
|
Idiopathic Familial Dystonia
|
Dystonia-Parkinsonism, Rapid-Onset
|
|
Fragments Of Torsion Dystonia
|
Dyt-Atp1a3
|
|
Rapid-Onset Dystonia Parkinsonism
|
Rodp
|
|
Dystonia, Type 12
|
Dystonia 3, Torsion, X-Linked
|
|
Idiopathic Non-Familial Dystonia
|
Symptomatic Torsion Dystonia
|
|
Dystonia Disorders
|
|
|
| Developmental And Epileptic Encephalopathy |
|
Encephalopathy, Developmental And Epileptic
|
|
|
| Brain Small Vessel Disease 1 |
|
Col4a1-Related Brain Small Vessel Disease With Hemorrhage
|
Col4a1-Related Familial Vascular Leukoencephalopathy
|
|
Col4a1-Related Retinal Arteriolar Tortuosity-Infantile Hemiparesis-Autosomal Dominant Leukoencephalopathy Syndrome
|
Autosomal Dominant Retinal Arteriolar Tortuosity, Infantile Hemiparesis, And Leukencephalopathy
|
|
Brain Small Vessel Disease With Axenfeld-Riegar Anomaly
|
Brain Small Vessel Disease With Hemorrhage
|
|
Brain Small Vessel Disease With Or Without Ocular Anomalies
|
Bsvd1
|
|
Infantile Hemiparesis
|
Leukoencephalopathy With Axenfeld-Riegar Anomaly
|
|
|
| Warburg Micro Syndrome 1 |
|
Warburg Micro Syndrome
|
Micro Syndrome
|
|
Warbm
|
WARBM1
|
|
Warburg Sjo Fledelius Syndrome
|
Warburg-Sjo-Fledelius Syndrome
|
|
Micro Syndrome 1
|
Microcephaly, Microcornea, Congenital Cataract, Intellectual Disability, Optic Atrophy And Hypogenitalism
|
|
|
| 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
|
|
|
| Infancy Electroclinical Syndrome |
|
|
| Microcephaly |
|
Microencephaly
|
Microcephalus
|
|
Microcephalic
|
Nanocephaly
|
|
Congenital Microcephaly
|
Brain Hypoplasia
|
|
Brain Nondevelopment
|
Cephalic Hypoplasia
|
|
Undeveloped Cerebrum
|
Undeveloped Brain
|
|
Micrencephalon
|
Micrencephaly
|
|
|
| Retinal Arteries, Tortuosity Of |
|
Retinal Arterial Tortuosity
|
Retinal Hemorrhage With Vascular Tortuosity
|
|
RATOR
|
Tortuosity Of Retinal Arteries
|
|
Retinal Arteriolar Tortuosity
|
Familial Isolated Retinal Arterial Tortuosity
|
|
Tortuosity, Arteries, Retinal
|
|
|
| Vasculopathy, Retinal, With Cerebral Leukoencephalopathy And Systemic Manifestations |
|
Retinal Vasculopathy With Cerebral Leukoencephalopathy And Systemic Manifestations
|
Crv
|
|
Rvcl
|
Rvcl-S
|
|
Vasculopathy, Retinal, With Cerebral Leukodystrophy
|
Retinopathy, Vascular, With Cerebral And Renal Involvement And Raynaud And Migraine Phenomena
|
|
Retinal Vasculopathy With Cerebral Leukodystrophy
|
Retinal Vasculopathy And Cerebral Leukoencephalopathy
|
|
Hereditary Vascular Retinopathy
|
Hvr
|
|
RVCLS
|
Cerebroretinal Vasculopathy, Hereditary
|
|
Cerebroretinal Vasculopathy
|
Herns
|
|
Vasculopathy, Retinal, With Cerebral Leukodystrophy, Formerly
|
Hereditary Cerebroretinal Vasculopathy
|
|
Hereditary Endotheliopathy, Retinopathy, Nephropathy, Stroke
|
Hereditary Systemic Angiopathy
|
|
Hsa
|
Retinal Vasculopathy With Cerebral Leukodystrophy With Systemic Manifestations
|
|
Adrvcl
|
Autosomal Dominant Retinal Vasculopathy With Cerebral Leukodystrophy
|
|
Hereditary Endotheliopathy With Retinopathy-Nephropathy-Stroke
|
Vascular Retinopathy With Cerebral And Renal Involvement And Raynaud And Migraine Phenomena
|
|
|
| Patent Foramen Ovale |
|
Atrial Septal Defect Within Oval Fossa
|
Foramen Ovale Patent
|
|
Ostium Secundum Atrial Septal Defect
|
Atrial Septal Defect, Ostium Secundum Type
|
|
Foramen Ovale, Patent
|
Defect, Patent Or Persistent, Ostium Secundum
|
|
Ostium Secundum Type Atrial Septal Defect
|
Persistent Ostium Secundum
|
|
Asd Ostium Secundum Type
|
Ostium Secundum Asd
|
|
Osasd
|
Asd, Ostium Secundum Type
|
|
Pfo - [Patent Foramen Ovale]
|
Open Foramen Ovale
|
|
Open Oval Foramen
|
Persistent Foramen Ovale
|
|
Secundum Atrial Septal Defect
|
|
|
| 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
|
|
|
| Dravet Syndrome |
|
Severe Myoclonic Epilepsy Of Infancy
|
Severe Myoclonic Epilepsy In Infancy
|
|
Smei
|
Epileptic Encephalopathy, Early Infantile, 6
|
|
DRVT
|
Developmental And Epileptic Encephalopathy 6a
|
|
Dee6a
|
Eiee6
|
|
Developmental And Epileptic Encephalopathy, 6
|
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
|
|
Infantile Severe Myoclonic Epilepsy
|
Epilepsy, Intractable Childhood, With Generalized Tonic-Clonic Seizures
|
|
|
| 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
|
|
|
| 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
|
|
|
| Early Infantile Epileptic Encephalopathy |
|
Early Infantile Epileptic Encephalopathy With Burst-Suppression
|
Early Infantile Epileptic Encephalopathy With Suppression Bursts
|
|
Eiee
|
Early Infantile Epileptic Encephalopathy With Suppression-Bursts
|
|
Ohtahara Syndrome
|
Encephalopathy, Epileptic, Early Infantile
|
|
|
