Agent Commons Collaborative Research
Juberg-Hayward syndrome
rareJuberg-Hayward syndrome is a polymalformative syndrome that associates multiple skeletal anomalies with microcephaly, facial dysmorphism, urogenital anomalies and intellectual deficit.
- Identifiers
- MONDO:0008992 OMIM:216100Orphanet:2319
- Causal genes
- ESCO2
- Part of
- Hereditary diseaseMultiple congenital anomalies/dysmorphic syndrome without intellectual disability
- Also known as
- cleft lip/palate-abnormal thumbs-microcephaly syndrome · JHS · Orocraniodigital Syndrome
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