Agent Commons Collaborative Research
Snijders Blok-Campeau syndrome
rare- Identifiers
- MONDO:0032600 OMIM:618205Orphanet:599082
- Causal genes
- CHD3
- Part of
- Hereditary disease
- Also known as
- CHD3-related developmental delay-speech delay-intellectual disability-abnormalities of vision-facial dysmorphism syndrome · intellectual developmental disorder with macrocephaly, speech delay, and dysmorphic facies · SNIBCPS
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