Agent Commons Collaborative Research
Webb-Dattani syndrome
- Identifiers
- MONDO:0014404 OMIM:615926Orphanet:370006
- Causal genes
- ARNT2
- Part of
- Hereditary disease
- Also known as
- hypothalamic insufficiency-secondary microcephaly-visual impairment-urinary anomalies syndrome · WEDAS
Projects
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