Disease #01881 (SCOTD (succinyl-CoA acetoacetate transferase deficiency (SCOTD)), OMIM:245050)

Official abbreviation SCOTD
Name succinyl-CoA acetoacetate transferase deficiency (SCOTD)
OMIM ID 245050
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene OXCT1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2019-03-09 15:41:33 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00080959 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - SCOTD Succinyl CoA:3-oxoacid CoA transferase deficiency (OMIM:245050) OXCT1 OXCT1 1 1 Daniel Trujillano
00226587 - - - M no United States Mexico - - - - SCOTD - OXCT1 OXCT1 1 1 Toshiyuki Fukao
00451603 3bINP-060 PubMed: Vela-Amieva 2024 - M no Mexico Mexican - - - - SCOTD Attention deficit hyperactivity disorder, mild intellectual disability, seizures OXCT1 OXCT1 1 1 Miriam Erandi Reyna-Fabián
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