Carpenter syndrome

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Summary

Literature (0)

DOID:0060234 - Carpenter syndrome

Disease Ontology Definition:An acrocephalosyndactylia characterized by craniosynostosis, acrocephaly, obesity, syndactyly and polydactyly.

Synonyms: acrocephalopolysyndactyly type II

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

: rab23, megf8

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0019012 - Carpenter syndrome

MONDO:0019012 - Carpenter syndrome

MIM:

MIM:201000 - CARPENTER SYNDROME 1; CRPT1
MIM:614976 - CARPENTER SYNDROME 2; CRPT2

MIM:201000 - CARPENTER SYNDROME 1; CRPT1

MIM:614976 - CARPENTER SYNDROME 2; CRPT2

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

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

Parent(s): acrocephalosyndactylia (is_a)