Rafiq syndrome

Summary

DOID:0081097 - Rafiq syndrome

Disease Ontology Definition:An autosomal recessive intellectual developmental disorder that is characterized by variably impaired intellectual and motor development, a characteristic facial dysmorphism, truncal obesity, and hypotonia and that has_material_basis_in homozygous mutation in the MAN1B1 gene on chromosome 9q34.

Synonyms: MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: man1b1

MIM:

MIM:614202 - RAFIQ SYNDROME; RAFQS

MIM:614202 - RAFIQ SYNDROME; RAFQS

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive intellectual developmental disorder (is_a)