Disease #02245 (MCOPS1 (microphthalmia, syndromic, type 1 (Lenz microphthalmia syndrome)), OMIM:309800)

Official abbreviation MCOPS1
Name microphthalmia, syndromic, type 1 (Lenz microphthalmia syndrome)
OMIM ID 309800
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked
Individuals reported having this disease 3
Phenotype entries for this disease -
Associated with 1 gene NAA10
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2023-12-28 13:53:52 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00060313 - - - M no - - - - - - ID, MCOPS1 - NAA10 NAA10 1 1 Bernt Popp
00063247 - PubMed: Forrester 2001 - M no - white - - - - ID, MCOPS1 - NAA10 NAA10 1 1 Bernt Popp
00063248 - PubMed: Forrester 2001 - M no - white - - - - ID, MCOPS1 - NAA10 NAA10 1 1 Bernt Popp
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