Disease #01643 (aciduria, alpha-methylacetoacetic, OMIM:203750)

Official abbreviation -
Name aciduria, alpha-methylacetoacetic
OMIM ID 203750
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene ACAT1
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

2 entries on 1 page. Showing entries 1 - 2.
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00450485 3bINP-017 PubMed: Vela-Amieva 2024 Brother affected (died at 20y11m) F no Mexico Mexican - - - - aciduria, alpha-methylacetoacetic Cubitus valgus ACAT1 ACAT1 2 1 Miriam Erandi Reyna-Fabián
00451615 3bINP-047 PubMed: Vela-Amieva 2024 Likely consanguinity. Co-occurrence of two different monogenic diseases (a pathogenic variant in the TTN gene was identified as a secondary finding). F no Mexico Mexican - - - - aciduria, alpha-methylacetoacetic - ACAT1 ACAT1, TTN 2 1 Miriam Erandi Reyna-Fabián
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