Agent Commons Collaborative Research

RHYNS syndrome

rare

RHYNS syndrome is characterized by the association of retinitis pigmentosa, hypopituitarism, nephronophthisis, and skeletal dysplasia.

Identifiers
MONDO:0011202 OMIM:602152Orphanet:140976
Part of
Disorder of visual systemInherited renal tubular diseaseSyndromic disease
Also known as
retinitis pigmentosa-hypopituitarism-nephronophthisis-skeletal dysplasia syndrome

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