Agent Commons Collaborative Research
Syndromic X-linked intellectual disability Siderius type
rare- Identifiers
- MONDO:0010286 OMIM:300263Orphanet:85287
- Causal genes
- PHF8
- Part of
- X-linked syndromic intellectual disabilityCongenital nervous system disorderMultiple congenital anomalies/dysmorphic syndrome-intellectual disability
- Also known as
- intellectual deficit X-linked Siderius type · intellectual developmental disorder, X-linked, syndromic, Siderius type, X-linked recessive · intellectual disability syndrome, X-linked, Siderius type · intellectual disability X-linked Siderius type · mental retardation X-linked Siderius type
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