|  Help  |  About  |  Contact Us

DO Term : primary autosomal recessive microcephaly 15 [DOID:0070277] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A primary autosomal recessive microcephaly characterized by impaired intellectual development with poor speech, progressive microcephaly, and appendicular spasticity that has_material_basis_in homozygous or compound heterozygous mutation in the MFSD2A gene on chromosome 1p34.
  • synonyms:
  • NEDMISBA,
  • neurodevelopmental disorder with progressive microcephaly, spasticity, and brain imaging abnormalities,
  • MCPH15,
  • 616486,
  • OMIM:616486
Quick Links:
 
Quick Links:
 

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents