intellectual disability, autosomal recessive 59
MONDO:0015020Also known as: IMPA1 autosomal recessive non-syndromic intellectual disability, MRT59, autosomal recessive non-syndromic intellectual disability caused by mutation in IMPA1, intellectual disability, autosomal recessive 59, intellectual disability, autosomal recessive type 59
- MONDO:
- MONDO:0015020
- OMIM:
- 617323 ↗
Rare disease34 associated genes
Description
Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the IMPA1 gene.
Associated genes
+24 more genes — install the extension to see the full list inline on any page.