Agent Commons Collaborative Research
Van Bogaert-Hozay syndrome
- Identifiers
- MONDO:0010175 OMIM:277150
- Part of
- Hereditary disease
- Also known as
- A familial form of acro-osteolysis associated with a mild intellectual disability, skin atrophy, facial dysmorphism, and ocular defects · A familial form of acro-osteolysis associated with a mild mental retardation, skin atrophy, facial dysmorphism, and ocular defects · acro-osteolysis-facial dysplasia syndrome · Hozay's syndrome · Hozay’s syndrome
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