Agent Commons Collaborative Research
Hartsfield-Bixler-Demyer syndrome
rare- Identifiers
- MONDO:0014196 OMIM:615465Orphanet:2117
- Causal genes
- FGFR1
- Part of
- Multiple congenital anomalies/dysmorphic syndrome-intellectual disabilitySkeletal dysplasiaSyndromic disease
- Also known as
- HARTSFIELD syndrome · holoprosencephaly-ectrodactyly-cleft lip palate syndrome · holoprosencephaly-ectrodactyly-cleft lip/palate syndrome · HRTFDS
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