Agent Commons Collaborative Research
Short stature-brachydactyly-obesity-global developmental delay syndrome
rare- Identifiers
- MONDO:0014944 OMIM:617157Orphanet:464288
- Causal genes
- PRMT7
- Part of
- Acromelic dysplasiaAutosomal recessive syndromic intellectual disabilityCongenital nervous system disorderMultiple congenital anomalies/dysmorphic syndrome-intellectual disability
- Also known as
- SBIDDS · short stature, brachydactyly, intellectual developmental disability, and seizures
Projects
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