Disease #04367 (PHPVAR (vitreous, primary, hyperplastic, persistent, autosomal recessive (PHPVAR)), OMIM:221900)

Official abbreviation PHPVAR
Name vitreous, primary, hyperplastic, persistent, autosomal recessive (PHPVAR)
OMIM ID 221900
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 4
Phenotype entries for this disease 1
Associated with 1 gene ATOH7
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00265313 PHPV Patient V-5 PubMed: Prasov 2012 6 generation family, 5 affected (previously reported in PubMed: Khaliq 2011) - yes Pakistan - - - - - PHPVAR persistent hyperplasia of the primary vitreous (PHPV, HP:0007968), gross nystagmus (HP:0000639) ATOH7 ATOH7 1 5 Jasmine Chen
00274336 V-1 PubMed: Gal 2014 5 generation family, 13 affected M yes (Israel) Bedouin - - - - EVR5, EVR;FEVR, ND, PHPVAR blindness (HP:0000618), phthisis bulbi (HP:0000667) - TSPAN12 1 13 Jasmine Chen
00274337 V-8 PubMed: Gal 2014 5 generation family, 13 affected M yes Israel Bedouin - - - - EVR5, EVR;FEVR, ND, PHPVAR total retinal detachment (HP:0000541) - TSPAN12 1 12 Jasmine Chen
00274354 IV:1 PubMed: Li 2019 4 generation family, 6 affected (2 severe, 4 mild) M no China - - - - - EVR5, EVR;FEVR, PHPVAR exudative vitreoretinopathy (HP:0030490), mild persistent hyperplasia of the primary vitreous (HP:0007968) - TSPAN12 1 6 Jasmine Chen
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