Disease #04670 (SORD (cataract, congenital?), OMIM:182500)

Official abbreviation SORD
Name cataract, congenital?
OMIM ID 182500
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene SORD
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:23 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00088183 NYS-008 PubMed: Thomas 2017, Journal: Thomas 2017 3-generation family, 3 affected (2F, M) F;M - United Kingdom (Great Britain) - - - - - SORD BCVA = 0.48LogMAR Horizontal and vertical jerk nystagmus Ptosis - CRYBA1 1 1 Mervyn Thomas
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