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RHYNS syndrome

Disease Export to PDF
Name:
RHYNS syndrome
Description:
A rare genetic, syndromic retinal disorder characterized by the association of retinitis pigmentosa, hypopituitarism, nephronophthisis, and skeletal dysplasia.
ORPHAcode:
140976
Synonyms:
Retinitis pigmentosa-hypopituitarism-nephronophthisis-skeletal dysplasia syndrome
XREF(s):
Orphanet
ICD-10
OMIM
MeSH
Analyte(s):
TMEM67
Created:
17 May 2022 - 02:46
Changed:
22 Jun 2023 - 16:14