Dimethylglycine dehydrogenase deficiency

about

Cloning of dimethylglycine dehydrogenase and a new human inborn error of metabolism, dimethylglycine dehydrogenase deficiency Molecular basis of dimethylglycine dehydrogenase deficiency associated with pathogenic variant H109R.[DMGDH gene-related dimethylglycine dehydrogenase deficiency in a case].

P921

Q24290887-17F81311-58EA-41B3-B541-FFC228735CC1 Q39266228-4105E65C-14C8-4B5F-BF10-6278BF990540 Q50205800-6967D73A-D611-479D-A149-0B015CD5CDD9

P921

Dimethylglycine dehydrogenase deficiency

Item

http://www.wikidata.org/entity/Q55783428

description

Dimethylglycine dehydrogenase ...... e fatigue and a fish-like odor

@en

name

Dimethylglycine dehydrogenase deficiency

@en

type

Item

label

Dimethylglycine dehydrogenase deficiency

@en

altLabel

DIMETHYLGLYCINE DEHYDROGENASE DEFICIENCY

@en

DIMETHYLGLYCINE DEHYDROGENASE DEFICIENCY; DMGDHD

@en

DMG dehydrogenase deficiency

@en

DMGDHD

@en

Dmgdh Deficiency

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prefLabel

Dimethylglycine dehydrogenase deficiency

@en

P1550

243343

http://www.w3.org/2001/XMLSchema#string

P2293

DMGDH

P279

inborn disorder of serine or glycine metabolism

P2888

Orphanet_243343

P2892

C1853892

http://www.w3.org/2001/XMLSchema#string

P31

Banaw

rare disease

P4229

E72.5

http://www.w3.org/2001/XMLSchema#string

P486

C565278

http://www.w3.org/2001/XMLSchema#string

P492

605850

http://www.w3.org/2001/XMLSchema#string

P5270

MONDO:0011610

http://www.w3.org/2001/XMLSchema#string