Search Ontology:
Human Disease

autosomal dominant microcephaly

Term ID
DOID:14725
Synonyms
Definition
A microcephaly that has_material_basis_in heterozygous mutation in an autosomal gene. https://www.ncbi.nlm.nih.gov/pubmed/3236353
References
Ontology
Human Disease   ( DOID:14725 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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