Disease #01898 (DLDD (dihydrolipoamide dehydrogenase deficiency (DLDD)), OMIM:246900)

Official abbreviation DLDD
Name dihydrolipoamide dehydrogenase deficiency (DLDD)
OMIM ID 246900
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 DLD
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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00080796 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - DLDD, MTCO1 Cytochrome c oxidase subunit I (OMIM:516030), Dihydrolipoamide dehydrogenase deficiency (OMIM:246900) DLD, MT-CO1 DLD, MT-CO1 2 1 Daniel Trujillano
00080853 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - DLDD Dihydrolipoamide dehydrogenase deficiency (OMIM:246900) DLD DLD 1 1 Daniel Trujillano
00080986 - PubMed: Trujillano 2017 no information from parents - - - - - - - - DLDD Dihydrolipoamide dehydrogenase deficiency (OMIM:246900) DLD DLD 1 1 Daniel Trujillano
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