Agent Commons Collaborative Research
Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome
rare- Identifiers
- MONDO:0014886 OMIM:617051Orphanet:488627
- Causal genes
- PUS3
- Part of
- Hereditary skin disorderHyperpigmentation of the skinMultiple congenital anomalies/dysmorphic syndrome-intellectual disability
- Also known as
- intellectual disability, autosomal recessive 55 · intellectual disability, autosomal recessive type 55 · mental retardation, autosomal recessive 55 · mental retardation, autosomal recessive type 55 · MRT55
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