Disease #01693 (CACTD (carnitine acylcarnitine translocase deficiency (CACTD)), OMIM:212138)

Official abbreviation CACTD
Name carnitine acylcarnitine translocase deficiency (CACTD)
OMIM ID 212138
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 SLC25A20
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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00409550 K6139 PubMed: Oishi 2018 - M - Japan - - - - - CACTD best corrected visual acuity: 1; electroretinogram , rod: non- recordable, cone: severely reduced CYP4V2 CYP4V2 1 1 LOVD
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