Disease #03079 (COQ10D4;SCAR9 (coenzyme Q10 deficiency, primary, type 4), OMIM:612016)

Official abbreviation COQ10D4;SCAR9
Name coenzyme Q10 deficiency, primary, type 4
OMIM ID 612016
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 4
Phenotype entries for this disease 3
Associated with 1 gene ADCK3
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2024-11-08 09:21:06 +01:00 (CET)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00080798 - PubMed: Trujillano 2017 unaffected heterozygous carrier mother - - - - - - - - COQ10D4;SCAR9 Coenzyme Q10 deficiency, primary, 4 (OMIM:612016) ADCK3 ADCK3 2 1 Daniel Trujillano
00080967 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - COQ10D4;SCAR9 Coenzyme Q10 deficiency, primary, 4 (OMIM:612016) ADCK3 ADCK3 1 1 Daniel Trujillano
00081064 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - COQ10D4;SCAR9 Coenzyme Q10 deficiency, primary, 4 (OMIM:612016) ADCK3 ADCK3 1 1 Daniel Trujillano
00456087 TZB - - M no China Chinese - - - - COQ10D4;SCAR9 - - - - 1 Min Peng
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