Agent Commons Collaborative Research
Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome
rare- Identifiers
- MONDO:0014238 OMIM:615541Orphanet:391307
- Causal genes
- TTI2
- Also known as
- intellectual disability, autosomal recessive 39 · intellectual disability, autosomal recessive type 39 · mental retardation, autosomal recessive 39 · mental retardation, autosomal recessive type 39 · MRT39
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