|  Help  |  About  |  Contact Us

DO Term : muscular dystrophy-dystroglycanopathy type B5 [DOID:0110635] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A congenital muscular dystrophy characterized by autosomal recessive inheritance of muscular dystrophy with variable penetrance of intellectual disability and structural brain abnormalities that has_material_basis_in homozygous or compound heterozygous mutation in the FKRP gene on chromosome 19q13.3.
  • synonyms:
  • FKRP-related congenital muscular dystrophy,
  • MDC1C,
  • congenital muscular dystrophy 1C,
  • muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5,
  • ORDO:52428,
  • muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type B, 5,
  • 606612,
  • OMIM:606612,
  • ICD10CM:G71.2,
  • MDDGB5
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