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Disease Ontology Browser
hypertelorism, microtia, facial clefting syndrome (DOID:14670)
Synonyms: Bixler Christian Gorlin syndrome; Bixler syndrome; Bixler-Christian-Gorlin syndrome; HMC syndrome; Hypertelorism-Microtia-Clefting Syndrome; Hypertelorism-microtia-facial clefting syndrome
Alt IDs: OMIM:239800, MESH:C537632, UMLS_CUI:C0220742
Definition: An autosomal recessive disease that is characterized by the combination of hypertelorism, cleft lip and palate and microtia.


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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
03/14/2017
MGI 6.08
The Jackson Laboratory