Neurodevelopmental disorder with or without variable movement or behavioral abnormalities

Preferred Label : Neurodevelopmental disorder with or without variable movement or behavioral abnormalities;

Symbol : NEDMAB;

Type : Phenotype, molecular basis known;

Prefixed ID : #619725;

Details

Origin ID

619725;

UMLS CUI

C5676908;

Genes related to phenotype
- Potassium channel, calcium-activated, intermediate/small conductance, subfamily n, member 2 [OMIM gene]
HPO term(s)
- Abnormal periventricular white matter morphology [HPO term]
- Anxiety [HPO term]
- Ataxia [HPO term]
- Attention deficit hyperactivity disorder [HPO term]
- Autistic behavior [HPO term]
- Autosomal dominant inheritance [HPO term]
- Bilateral tonic-clonic seizure [HPO term]
- Bradykinesia [HPO term]
- Childhood onset [HPO term]
- Chorea [HPO term]
- Cogwheel rigidity [HPO term]
- Delayed CNS myelination [HPO term]
- Delayed speech and language development [HPO term]
- Dilated third ventricle [HPO term]
- Dyskinesia [HPO term]
- Dystonia [HPO term]
- Global developmental delay [HPO term]
- Infantile onset [HPO term]
- Intellectual disability [HPO term]
- Intention tremor [HPO term]
- Microcephaly [HPO term]
- Motor delay [HPO term]
- Motor tics [HPO term]
- Myoclonus [HPO term]
- Nocturnal seizures [HPO term]
- Panic attack [HPO term]
- Parkinsonism [HPO term]
- Psychosis [HPO term]
- Resting tremor [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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