Disease #01678 (MCC2D (3-methylcrotonyl CoA carboxylase 2 deficiency (MCC2D)), OMIM:210210)

Official abbreviation MCC2D
Name 3-methylcrotonyl CoA carboxylase 2 deficiency (MCC2D)
OMIM ID 210210
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 1 gene MCCC2
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

4 entries on 1 page. Showing entries 1 - 4.
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00181036 - - - - - - - - - - - MCC2D - MCCC2 MCCC2 2 1 Belen Perez
00181037 - - - - - - - - - - - MCC2D - MCCC2 MCCC2 2 1 Belen Perez
00403761 MCC019 PubMed: Stucki 2009 2-generation family, 1 affected, unaffected heterozygous carrier parents - yes Switzerland - - - - - MCC2D see paper; ..., failure to thrive MCCC2 MCCC2 1 1 Johan den Dunnen
00451602 3bINP-059 PubMed: Vela-Amieva 2024 Likely consanguinity M no Mexico Mexican - - - - MCC2D - MCCC2 MCCC2 1 1 Miriam Erandi Reyna-Fabián
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