Short sleep, familial natural, 2

Preferred Label : Short sleep, familial natural, 2;

Symbol : FNSS2;

CISMeF acronym : FNSS2;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the beta-1-adrenergic receptor gene (ADRB1, 109630.0003);

Prefixed ID : #618591;

Détails

Origin ID

618591;

UMLS CUI

C5231420;

Genes related to phenotype
- Beta-1-adrenergic receptor [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Shortened sleep cycle [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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