Baller-Gerold syndrome

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Echinobase

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:

Echinobase 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

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)