The PAN Foundation and Patient Advocate Foundation announced a strategic merger in March 2026. In the meantime, nothing is changing for patients. You can continue to apply for and use financial assistance from the PAN Foundation through panapply.org or by calling us at 1-866-316-7263. You can learn more about the announcement at uniting.patientadvocate.org.
Diagnosis codes
ICD-10: H31.21, H35.3110, H35.3111, H35.3112, H35.3113, H35.3114, H35.3120, H35.3121, H35.3122, H35.3123, H35.3124, H35.3130, H35.3131, H35.3132, H35.3133, H35.3134, H35.3190, H35.3191, H35.3192, H35.3193, H35.3194, H35.3210, H35.3211, H35.3212, H35.3213, H35.3220, H35.3221, H35.3222, H35.3223, H35.3230, H35.3231, H35.3232, H35.3233, H35.3290, H35.3291, H35.3292, H35.3293, H35.351, H35.352, H35.353, H35.359, H35.361, H35.362, H35.363, H35.369, H35.371, H35.372, H35.373, H35.379, H35.50, H35.51, H35.52, H35.53 H35.54, H35.89, H44.20, H44.21, H44.22, H44.23, H44.2A1, H44.2A2, H44.2A3, H44.2A9, H47.21, H47.211, H47.212, H47.213, H47.219, H47.22
About the disease
Inherited retinal disease (IRD), also known as inherited retinal disorder, is a disorder caused by an inherited gene mutation which can result in vision loss or blindness. IRD is a rare disease that affects the nervous system. Subtypes include retinitis pigmentosa, choroideremia, leber congenital amaurosis, juvenile macular degeneration and cone rod dystrophy.
Source: National Institutes of Health
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