OBO ID: DOID:0070294
Term Name: primary autosomal recessive microcephaly 10 Search Ontology:
Synonyms:
  • MCPH10
Definition: A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the ZNF335 gene on chromosome 20q13. https://www.ncbi.nlm.nih.gov/pubmed/23178126
References:
Ontology: Human Disease   (DOID:0070294)
OTHER primary autosomal recessive microcephaly 10 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ZNF335 Microcephaly 10, primary, autosomal recessive 615095
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None