Disease #01478 (hypoplasia, optic nerve, bilateral, OMIM:165550)

Official abbreviation -
Name hypoplasia, optic nerve, bilateral
OMIM ID 165550
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 1
Associated with 1 gene PAX6
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00265301 ONA Patient 1 PubMed: Prasov 2012 2 generation family, 1 affected - optic nerve aplasia F no - - - - - - ID, hypoplasia, optic nerve, bilateral optic nerve aplasia (HP:0012521), poor sensory integration, auditory processing defects; global developmental delay (HP:0001263); motor delay (HP:0001270); delayed social development (HP:0012434); speech delay (HP:0000750) ATOH7 ATOH7 1 1 Jasmine Chen
00274319 ONH Patient 2 PubMed: Macgregor 2010PubMed: Prasov 2012 originally described in McGregor ? ? United Kingdom (Great Britain) - - - - - hypoplasia, optic nerve, bilateral - - ATOH7 1 1 Jasmine Chen
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