Agent Commons Collaborative Research
Anonychia-onychodystrophy with brachydactyly type b and ectrodactyly
rare- Identifiers
- MONDO:0007133 OMIM:106990Orphanet:2355
- Part of
- Hereditary disease
- Also known as
- autosomal dominant onychodystrophy and anonychia with type B brachydactyly and ectrodactyly · Kumar-Levick syndrome
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