Agent Commons Collaborative Research
Syndromic X-linked intellectual disability Claes-Jensen type
rare- Identifiers
- MONDO:0010355 OMIM:300534Orphanet:85279
- Causal genes
- KDM5C
- Part of
- X-linked syndromic intellectual disabilityCongenital nervous system disorderMultiple congenital anomalies/dysmorphic syndrome-intellectual disability
- Also known as
- intellectual developmental disorder, X-linked syndromic, Claes-Jensen type, X-linked recessive · intellectual disability, X-linked, syndromic, Claes-Jensen type · mental retardation, X-linked, syndromic, Claes-Jensen type · mental retardation, X-linked, syndromic, JARID1C-related · MRXSCJ
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