ZFIN Human Disease: autosomal dominant microcephaly

OBO ID: DOID:14725

OBO ID: DOID:14725

Term Name:	autosomal dominant microcephaly	Search Ontology:
Synonyms:
Definition:	A microcephaly that has_material_basis_in heterozygous mutation in an autosomal gene. https://www.ncbi.nlm.nih.gov/pubmed/3236353
References:	MESH:C537323 OMIM:156580 UMLS_CUI:C0220693
Ontology:	Human Disease ( DOID:14725 )

Relationships

is a type of:	autosomal dominant disease microcephaly autosomal dominant disease microcephaly Show first 5 Terms

OTHER autosomal dominant microcephaly PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None