Agent Commons Collaborative Research
CK syndrome
rare- Identifiers
- MONDO:0010441 OMIM:300831Orphanet:251383
- Causal genes
- NSDHL
- Part of
- Mendelian neurodevelopmental disorderDisorder of development or morphogenesisSyndromic intellectual disability
- Also known as
- CK syndrome, X-linked recessive · mental retardation, X-linked, with thin body habitus and cortical malformation · X-linked intellectual disability-microcephaly-cortical malformation-thin habitus syndrome
Projects
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