Retinitis Pigmentosa 36 (RP36)

Alias:

Rp36

Retinitis Pigmentosa, Type 36

Retinitis Pigmentosa-36

Favorite

Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Retinitis Pigmentosa 36, also known as rp36, is related to mitochondrial dna-associated leigh syndrome and parkinson disease, mitochondrial. An important gene associated with Retinitis Pigmentosa 36 is PRCD (Photoreceptor Disc Component). Affiliated tissues include retina and eye, and related phenotypes are rod-cone dystrophy and optic disc pallor

Related ID：

MALACARDS：RTN065

OMIM：610599

MESH：C566431