Mirhosseini-Holmes-Walton syndrome

Mirhosseini–Holmes–Walton syndrome
Synonyms	Pigmentary retinopathy-intellectual disability syndrome
Classification and external resources
OMIM	268050
DiseasesDB	32623
Orphanet	3084
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Mirhosseini–Holmes–Walton syndrome is a syndrome which involves retinal degeneration, cataract, microcephaly, and mental retardation. It was first characterized in 1972.

There is evidence that this syndrome has a different mutation in the same gene as Cohen syndrome.