Disease #05622 (AN1 (aniridia, type 1 (cataract with late-onset corneal dystrophy)), OMIM:106210)

Official abbreviation AN1
Name aniridia, type 1 (cataract with late-onset corneal dystrophy)
OMIM ID 106210
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene PAX6
Associated tissues -
Disease features autosomal dominant
Remarks -
Date created 2019-07-12 09:07:29 +02:00 (CEST)
Date last edited 2023-12-23 15:14:09 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00371662 178813 - - M ? Germany - - - - - AN1 (+) Abnormality of the lens,(+) Cataract PAX6 PAX6 1 1 Andreas Laner
00382120 241 PubMed: Patel 2019 - ? - United Kingdom (Great Britain) - - - - - AN1 anterior segment developmental anomalies including glaucoma; MIM, 106210 PAX6 PAX6 1 1 LOVD
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