alopecia-mental retardation syndrome 1

Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary

Literature (0)

DOID:0080628 - alopecia-mental retardation syndrome 1

Disease Ontology Definition:An alopecia-mental retardation syndrome that has_material_basis_in homozygous mutation in the AHSG gene on chromosome 3q27.

Synonyms:

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

: ahsg

MIM:

MIM:203650 - ALOPECIA-INTELLECTUAL DISABILITY SYNDROME 1; APMR1

MIM:203650 - ALOPECIA-INTELLECTUAL DISABILITY SYNDROME 1; APMR1

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

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

Parent(s): alopecia-mental retardation syndrome (is_a), autosomal recessive disease (is_a)