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Hartsfield-Bixler-Demyer syndrome
Disease Summary
Associated Targets (1)
Tclin
1
Uniprot Description A syndrome characterized by the triad of holoprosencephaly, ectrodactyly, and cleft/lip palate. Profound mental retardation is also present. Multiple other congenital anomalies usually occur.
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Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
MESH:C564484
OMIM:615465
Orphanet:2117
SCTID:766032007
UMLS:C1845146
MONDO:0014196
High level summary of knowledge for a disease, including descriptions and datasource references.