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| Term | hypertelorism, microtia, facial clefting syndrome | ID (Ontology) | DOID:14670 (Human Disease) |
| Definition | A syndrome that is characterized by the combination of hypertelorism, cleft lip and palate and microtia. | ||
| Also Known As | "Bixler Christian Gorlin syndrome" ; "Bixler syndrome" ; "Bixler-Christian-Gorlin syndrome" (for all, see Synonyms field below) | ||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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No relevant statements available
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autosomal genetic disease |__autosomal recessive disease__ disease | |__syndrome_____________________| hypertelorism, microtia, facial clefting syndrome |
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| Is a |
autosomal recessive disease syndrome |
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External Crossreferences & Linkouts
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GARD:897 MESH:C537632 MIM:239800 ORDO:2213 SNOMEDCT_US_2023_03_01:721836009 UMLS_CUI:C0220742 |
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