Disease #01625 (ACADSD (Acyl-CoA dehydrogenase, short-chain, deficiency of), OMIM:201470)

Official abbreviation ACADSD
Name Acyl-CoA dehydrogenase, short-chain, deficiency of
OMIM ID 201470
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene ACADS
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

3 entries on 1 page. Showing entries 1 - 3.
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00181027 - - - - - - - - - - - ACADSD - ACADS ACADS 2 1 Belen Perez
00181052 - - - - - - - - - - - ACADSD - ACADS ACADS 2 1 Belen Perez
00451598 3bINP-052 PubMed: Vela-Amieva 2024 - F no Mexico Mexican - - - - ACADSD Blue sclerae ACADM ACADM 1 1 Miriam Erandi Reyna-Fabián
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