Disease #03598 (Hypermethioninemia due to adenosine kinase deficiency, OMIM:614300)

Official abbreviation -
Name Hypermethioninemia due to adenosine kinase deficiency
OMIM ID 614300
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 2
Associated with 1 gene ADK
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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00081060 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - Hypermethioninemia due to adenosine kinase deficiency Hypermethioninemia due to adenosine kinase deficiency (OMIM:614300) ADK ADK 1 1 Daniel Trujillano
00081083 - PubMed: Trujillano 2017 unaffected heterozygous carrier parents - - - - - - - - Hypermethioninemia due to adenosine kinase deficiency Hypermethioninemia due to adenosine kinase deficiency (OMIM:614300) ADK ADK 1 1 Daniel Trujillano
00266330 - - - - - - - - - - - Hypermethioninemia due to adenosine kinase deficiency - MAT1A MAT1A 1 1 Gemeinschaftspraxis für Humangenetik Dresden
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