Ocular albinism with sensorineural deafness

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
OCULAR ALBINISM WITH LATE-ONSET SENSORINEURAL DEAFNESS
1000
AP3D1 Unknown — Orphanet
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Ocular albinism with sensorineural deafness.
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Early-onset severe hermansky-pudlak syndrome with hearing loss due to ap3d1 deficiency 1 shared geneAP3D1 Related via 1 shared gene including AP3D1. hermansky-pudlak syndrome 10 1 shared geneAP3D1 Related via 1 shared gene including AP3D1. X-linked ocular abinism 1 shared geneAP3D1 Related via 1 shared gene including AP3D1. Hermansky-pudlak syndrome 1 shared geneAP3D1 Related via 1 shared gene including AP3D1. Emphysema 1 shared geneAP3D1 Related via 1 shared gene including AP3D1.