Disease #02120 (MAHCC (aciduria, methylmalonic, and homocystinuria, cblC type (MAHCC)), OMIM:277400)

Official abbreviation MAHCC
Name aciduria, methylmalonic, and homocystinuria, cblC type (MAHCC)
OMIM ID 277400
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 2 genes MMACHC, PRDX1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2020-07-09 16:30:16 +02:00 (CEST)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00306194 92 - - M - China - - - - - MAHCC - MMACHC MMACHC 2 1 Sha Hong
00311128 CHU-12122 PubMed: Guéant 2018 - F - - white 00y01m - - - MAHCC see paper; ... - CCDC163P, MMACHC, PRDX1 3 1 Johan den Dunnen
00311129 WG-3838 PubMed: Guéant 2018 - F - Japan;Korea - 00y02m - - - MAHCC - - CCDC163P, MMACHC, PRDX1 3 1 Johan den Dunnen
00311130 WG-4152 PubMed: Guéant 2018 - M - - white >59y - - - MAHCC - - CCDC163P, MMACHC, PRDX1 3 1 Johan den Dunnen
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