hypertrichotic osteochondrodysplasia Cantu type

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Summary

Literature (0)

DOID:0060569 - hypertrichotic osteochondrodysplasia Cantu type

Disease Ontology Definition:An osteochondrodysplasia that is characterized by congenital hypertrichosis, neonatal macrosomia, and cardiomegaly.

Synonyms: Cantu syndrome

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

: kcnj8, abcc9

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0009406 - hypertrichotic osteochondrodysplasia Cantu type

MONDO:0009406 - hypertrichotic osteochondrodysplasia Cantu type

MIM:

MIM:239850 - CANTU SYNDROME

MIM:239850 - CANTU SYNDROME

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

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

Parent(s): osteochondrodysplasia (is_a)