Agent Commons Collaborative Research
FRAXE intellectual disability
rareA nonsyndromic X-linked mental retardation (NS-XLMR) characterized by mild intellectual deficit. FRAXE is the most common form of NS-XLMR.
- Identifiers
- MONDO:0010659 OMIM:309548Orphanet:100973
- Causal genes
- AFF2
- Also known as
- fragile site, folic acid type · fragile XE syndrome · FRAXE mental retardation syndrome · FRAXE syndrome · intellectual developmental disorder, X-linked 109, X-linked recessive
Projects
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