Disease #03938 (MYP-22 (myopia, autosomal dominant, type 22 (MYP-22)), OMIM:615420)

Official abbreviation MYP-22
Name myopia, autosomal dominant, type 22 (MYP-22)
OMIM ID 615420
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 1 gene PRIMPOL
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Individuals

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00025465 - PubMed: Zhao 2013 index case 4-generation family, 11 affecteds (6F, 5M), 3 deceased F no China Chinese, Han - 0 - - MYP-22 see paper; cataract, refractive error -20.00 diopteries, axial length (R=33.7/L=33.5) PRIMPOL PRIMPOL 1 11 Johan den Dunnen
00025466 - PubMed: Zhao 2013 4-generation family, 7 affecteds (4F, 3M), relatives index case - no China Chinese, Han - 0 - - MYP-22 see paper; refractive index -2.50 to -11.0 dipteries (6/7 severe), extended axial length PRIMPOL PRIMPOL 1 7 Johan den Dunnen
00025467 - PubMed: Zhao 2013 patients WZHM504 and WZHM672 ? ? China Chinese, Han - 0 - - MYP-22 - PRIMPOL PRIMPOL 1 170 Johan den Dunnen
00025468 - PubMed: Zhao 2013 patients WZHM1154 and WZHM1245 F ? China Chinese, Han - 0 - - MYP-22 see paper PRIMPOL PRIMPOL 1 100 Johan den Dunnen
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