class of disease | Q112193867 |
rare disease | Q929833 |
eye disease | Q3041498 |
fundus dystrophy | Q5811451 |
autosomal dominant disease | Q18553439 |
P699 | Disease Ontology ID | DOID:0111541 |
P2888 | exact match | http://identifiers.org/doid/DOID:0111541 |
http://purl.obolibrary.org/obo/DOID_0111541 | ||
http://www.orpha.net/ORDO/Orphanet_251295 | ||
P4229 | ICD-10-CM | H35.5 |
P7807 | ICD-11 (foundation) | 1278139412 |
P665 | KEGG ID | H01088 |
P5270 | Mondo ID | MONDO_0008246 |
P492 | OMIM ID | 172870 |
172870 | ||
P1550 | Orphanet ID | 251295 |
P2892 | UMLS CUI | C1868310 |
P11430 | UniProt disease ID | DI-02166 |
P2293 | genetic association | CRB1 | Q18037166 |
P5008 | on focus list of Wikimedia project | WikiProject Medicine | Q4099686 |
Q46825575 | A familial case of pigmented paravenous retinochoroidal atrophy with asymmetrical fundus manifestations. |
Q99414603 | A mutation in CRX causing pigmented paravenous retinochoroidal atrophy |
Q54994458 | A rare case of unifocal, unilateral pigmented paravenous retinochoroidal atrophy (PPRCA). |
Q35098498 | A rare presentation of pigmented paravenous retinochoroidal atrophy |
Q101466081 | Association of pigmented paravenous retinochoroidal atrophy (PPRCA) with a pathogenic variant in the HK1 gene |
Q90260024 | Asymmetry in Pigmented Paravenous Retinochoroidal Atrophy |
Q37296819 | Bilateral macular coloboma and pigmented paravenous retinochoroidal atrophy |
Q39397019 | Concurrent retinitis pigmentosa and pigmented paravenous retinochoroidal atrophy phenotypes in the same patient |
Q46318665 | Correlation of lines of increased autofluorescence in macular dystrophy and pigmented paravenous retinochoroidal atrophy by optical coherence tomography |
Q58225967 | Five cases of pigmented paravenous retinochoroidal atrophy in dogs |
Q46175352 | Fundus autofluorescence and optical coherence tomography findings in pigmented paravenous retinochoroidal atrophy |
Q41532532 | Hereditary Pigmented Paravenous Retinochoroidal Atrophy |
Q44358413 | Indocyanine green angiography in pigmented paravenous retinochoroidal atrophy. |
Q39122787 | Inflammatory pigmented paravenous retinochoroidal atrophy |
Q42145802 | Inflammatory pigmented paravenous retinochoroidal atrophy |
Q91969767 | Macular involvement in a pigmented paravenous retinochoroidal atrophy |
Q100943088 | Multimodal imaging of pigmented paravenous retinochoroidal atrophy |
Q50779186 | Natural course of ocular function in pigmented paravenous retinochoroidal atrophy. |
Q88716322 | Optical Coherence Tomography Angiography of Pigmented Paravenous Retinochoroidal Atrophy |
Q54310194 | Pattern of inner retinal layers involvement in pigmented paravenous retinochoroidal atrophy as determined by SD-OCT: case report. |
Q88407296 | Pigmented Paravenous Retinochoroidal Atrophy |
Q89618017 | Pigmented Paravenous Retinochoroidal Atrophy |
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Q40258881 | Pigmented paravenous retinochoroidal atrophy |
Q64246249 | Pigmented paravenous retinochoroidal atrophy |
Q70553335 | Pigmented paravenous retinochoroidal atrophy |
Q70688764 | Pigmented paravenous retinochoroidal atrophy |
Q44211960 | Pigmented paravenous retinochoroidal atrophy (PPRA). |
Q72867944 | Pigmented paravenous retinochoroidal atrophy (PPRCA) with optic disc drusen |
Q38219975 | Pigmented paravenous retinochoroidal atrophy (Review). |
Q93035558 | Pigmented paravenous retinochoroidal atrophy associated with Vogt-Koyanagi-Harada disease: a case report |
Q92547323 | Pigmented paravenous retinochoroidal atrophy associated with unilateral cystoid macular oedema |
Q67779460 | Pigmented paravenous retinochoroidal atrophy in a 68-year-old man |
Q51271613 | Pigmented paravenous retinochoroidal atrophy with macular involvement. |
Q35566031 | Pigmented paravenous retinochoroidal atrophy. A literature review supported by seven cases |
Q68027736 | Pigmented paravenous retinochoroidal atrophy. Discordant expression in monozygotic twins |
Q55327265 | Pigmented paravenous retinochoroidal atrophy: a case report. |
Q34104783 | Pigmented paravenous retinochoroidal atrophy: a literature review supported by a unique case and insight |
Q44747165 | Pigmented paravenous retinochoroidal atrophy: a nosologic entity? |
Q74192637 | Pigmented paravenous retinochoroidal atrophy: evidence of progression to macular involvement in a family with a 42-year history |
Q67260793 | Progressive Nature of Pigmented Paravenous Retinochoroidal Atrophy |
Q90867988 | Rare case of simultaneous manifestation of pigmented paravenous retinochoroidal atrophy and retinitis pigmentosa in contralateral eye |
Q93565103 | Rubeola retinopathy and pigmented paravenous retinochoroidal atrophy |
Q34270261 | SD-OCT in pigmented paravenous retinochoroidal atrophy |
Q36349967 | Unilateral Pigmented Paravenous Retinochoroidal Atrophy Associated With Presumed Ocular Tuberculosis. |
Q46938165 | Unilateral pigmented paravenous retinochoroidal atrophy |
Q47106929 | Unilateral pigmented paravenous retinochoroidal atrophy with retinitis pigmentosa in the contralateral eye: A case report |
Q91702868 | Use of Wide-Field Fundus Camera, Fundus Autofluorescence, and OCT in Cases of Pigmented Paravenous Retinochoroidal Atrophy |
Q97093125 | [A case of pigmented paravenous retinochoroidal atrophy with cystoid macular edema] |
Q53061776 | [Pigmented Paravenous Retinochoroidal Atrophy]. |
Q85855974 | [Pigmented paravenous retinochoroidal atrophy--a case report] |
Q18037166 | CRB1 | genetic association | P2293 |
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