Disease #02903 (MCOPS5 (microphthalmia, syndromic, type 5 (dystrophy, retinal, early onset)), OMIM:610125)

Official abbreviation MCOPS5
Name microphthalmia, syndromic, type 5 (dystrophy, retinal, early onset)
OMIM ID 610125
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene OTX2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2023-12-23 15:02:48 +01:00 (CET)


Individuals

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00037524 - - - M no El Salvador Hispanic - - - - MCOPS5 Anophthalmia Short Stature Intellectual Disability Cerebral Palsy Cryptorchidism OTX2 OTX2 1 1 Elena Semina
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