Baller-Gerold syndrome

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Summary

Literature (0)

DOID:0050654 - Baller-Gerold syndrome

Disease Ontology Definition:A synostosis characterized by coronal craniosynostosis, short stature, and aplasia or hypoplasia of the radial bone.

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

: recql4

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0009039 - Baller-Gerold syndrome

MONDO:0009039 - Baller-Gerold syndrome

MIM:

MIM:218600 - BALLER-GEROLD SYNDROME; BGS

MIM:218600 - BALLER-GEROLD SYNDROME; BGS

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

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

Parent(s): synostosis (is_a)