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

• OMIM:615095

Ontology

Human Disease   ( DOID:0070294 )