Disease #01682 (SHEP6 (pigmentation, skin/hair/eye, variation in, type 6 (SHEP-6)), OMIM:210750)

Official abbreviation SHEP6
Name pigmentation, skin/hair/eye, variation in, type 6 (SHEP-6)
OMIM ID 210750
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene SLC24A4
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00409539 K6782 PubMed: Oishi 2018 - F - Japan - - - - - SHEP6 best corrected visual acuity: 0.6; electroretinogram , rod: mildly reduced, cone: mildly reduced CYP4V2 CYP4V2 2 1 LOVD
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