/RHYNS syndrome

RHYNS syndrome

Rare Disease

MONDO:0011202

Also Known As

RHYNS syndromeretinitis pigmentosa-hypopituitarism-nephronophthisis-skeletal dysplasia syndromeretinitis pigmentosa syndromeretinitis pigmentosa, hypopituitarism, nephronophthisis, and mild skeletal dysplasia

Definition

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

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

TMEM67 ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

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RHYNS syndrome

Also Known As

Definition

Patient-Friendly Information

Associated Genes

External Resources

OMIM

Orphanet

GARD

Related Diseases