Search Ontology:
Human Disease

primary autosomal recessive microcephaly 10

Term ID
DOID:0070294
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 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models