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Ontology Browser
Term:
Familial Infantile Convulsions and Paroxysmal Choreoathetosis (DOID:9007283)
Annotations: Rat: (2) Mouse: (2) Human: (5) Chinchilla: (2) Bonobo: (3) Dog: (2) Squirrel: (2) Pig: (2) Naked Mole-rat: (2) Green Monkey: (2)
Parent Terms Term With Siblings Child Terms
benign familial infantile epilepsy +     
Dyskinesias +     
visual epilepsy +     
Adams Nance Syndrome 
Alopecia-Mental Retardation Syndrome with Convulsions and Hypergonadotropic Hypogonadism 
Ataxia +   
Athetosis +   
autosomal dominant intellectual developmental disorder 6  
autosomal dominant nocturnal frontal lobe epilepsy 4  
Baraitser Rodeck Garner syndrome 
benign familial infantile seizures 1  
benign familial infantile seizures 2  
benign familial infantile seizures 3  
benign familial infantile seizures 4 
benign familial infantile seizures 5  
benign familial infantile seizures 6  
Bobble-Head Doll Syndrome 
Catalepsy  
Cerebroretinal Microangiopathy with Calcifications and Cysts +   
choreatic disease +   
chromosome 15q13.3 microdeletion syndrome  
cold-induced sweating syndrome +   
Copper Deficiency, Familial Benign 
craniosynostosis 2  
Drug-Induced Dyskinesia +   
Dyskinesia with Orofacial Involvement +   
Dyskinesias, Seizures, and Intellectual Developmental Disorder  
Dysmyelination with Jaundice 
dystonia +   
EAST syndrome  
Familial Convulsive Disorder with Prenatal or Early Onset 
Familial Infantile Convulsions and Paroxysmal Choreoathetosis  
Hyper-Beta-Alaninemia 
Hyperkinesis +   
Hyperleucine-Isoleucinemia 
hypermethioninemia due to adenosine kinase deficiency  
Hypokinesia +   
hypoparathyroidism-retardation-dysmorphism syndrome  
infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly  
Infantile-Onset Limb and Orofacial Dyskinesia  
lingual-facial-buccal dyskinesia 
Mental Retardation, Keratoconus, Febrile Seizures, and Sinoatrial Block 
Methionine Malabsorption Syndrome 
Microcephaly Pontocerebellar Hypoplasia Dyskinesia 
Microcephaly Seizures Genital Hypoplasia 
Microcephaly Seizures Mental Retardation Heart Disorders 
Microcephaly Sparse Hair Mental Retardation Seizures 
microcephaly, seizures, and developmental delay  
Microcephaly, Short Stature, and Polymicrogyria with or without Seizures  
Mirror Movements 1  
Mirror Movements 2  
Mirror Movements 3  
Mirror Movements 4  
Muller Barth Menger Syndrome 
multiple congenital anomalies-hypotonia-seizures syndrome +   
myoclonic-atonic epilepsy  
Myoclonus +   
Neurodevelopmental Disorder with Hypotonia, Microcephaly, and Seizures   
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE  
Occipital Cortical Malformations  
optic atrophy 10  
Pachygyria with Mental Retardation, Seizures, and Arachnoid Cysts  
Paroxysmal Exertion-Induced Dyskinesia and Hemolytic Anemia 
Partington syndrome  
Perniola Krajewska Carnevale Syndrome 
PHGDH deficiency  
Primary Aldosteronism, Seizures, and Neurologic Abnormalities  
PSAT deficiency  
Psychomotor Agitation +   
Qazi Markouizos syndrome 
Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal  
Seizures, Cortical Blindness, and Microcephaly Syndrome  
Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures  
Smith-Kingsmore Syndrome  
syndromic X-linked intellectual disability 5  
syndromic X-linked intellectual disability type 10  
Synkinesis +  
Tics  
Tranebjaerg Svejgaard syndrome 
Tremor +   
White-Sutton syndrome  
X-linked mental retardation Gustavson type  

Synonyms
Exact Synonyms: CONVULSIONS, FAMILIAL INFANTILE, WITH PAROXYSMAL CHOREOATHETOSIS ;   ICCA ;   ICCA syndrome ;   PAROXYSMAL KINESIGENIC DYSKINESIA WITH INFANTILE CONVULSIONS ;   PKD/IC
Primary IDs: MESH:C535522
Alternate IDs: MIM:602066

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