multiple acyl-CoA dehydrogenase deficiency (Q1403045)

From The Right Wiki
Jump to navigationJump to search
medical condition
  • MAD deficiency
  • MADD
  • electron transfer flavoprotein deficiency
  • electron transfer flavoprotein ubiquinone oxidoreductase deficiency
  • glutaric acidemia type 2
  • glutaric aciduria type 2
  • Glutaric acidaemia type 2
  • Glutaric Acidemia 2B
  • Glutaric Aciduria 2
  • Etfb Deficiency
  • Glutaric Acidemia 2C
  • Glutaric Acidemia 2A
  • Multiple Acyl Coenzyme A Dehydrogenase Deficiency
  • MULTIPLE ACYL-CoA DEHYDROGENASE DEFICIENCY
  • MULTIPLE ACYL-CoA DEHYDROGENASE DEFICIENCY; MADD
  • Ethylmalonic-Adipicaciduria
  • Etfdh Deficiency
  • Etfa Deficiency
  • Glutaric Acidemia 2
  • Ga 2
  • Glutaric Aciduria, Type 2
Language Label Description Also known as
English
multiple acyl-CoA dehydrogenase deficiency
medical condition
  • MAD deficiency
  • MADD
  • electron transfer flavoprotein deficiency
  • electron transfer flavoprotein ubiquinone oxidoreductase deficiency
  • glutaric acidemia type 2
  • glutaric aciduria type 2
  • Glutaric acidaemia type 2
  • Glutaric Acidemia 2B
  • Glutaric Aciduria 2
  • Etfb Deficiency
  • Glutaric Acidemia 2C
  • Glutaric Acidemia 2A
  • Multiple Acyl Coenzyme A Dehydrogenase Deficiency
  • MULTIPLE ACYL-CoA DEHYDROGENASE DEFICIENCY
  • MULTIPLE ACYL-CoA DEHYDROGENASE DEFICIENCY; MADD
  • Ethylmalonic-Adipicaciduria
  • Etfdh Deficiency
  • Etfa Deficiency
  • Glutaric Acidemia 2
  • Ga 2
  • Glutaric Aciduria, Type 2

Statements

OMIM ID
231680
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0060358
NCI Thesaurus ID
C99102
mapping relation type
Q39893184 (Deleted Item)
1 reference
stated in
Q55345445 (Deleted Item)
retrieved
28 July 2018
Mondo ID
MONDO_0009282
C84907
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0060358
subclass of
Q1758393 (Deleted Item)
1 reference
stated in
Disease Ontology
retrieved
29 November 2020
Disease Ontology ID
DOID:0060358
Q55787302 (Deleted Item)
1 reference
stated in
Q55345445 (Deleted Item)
retrieved
28 July 2018
Mondo ID
MONDO_0009282
Q55786145 (Deleted Item)
1 reference
stated in
Q55345445 (Deleted Item)
retrieved
28 July 2018
Mondo ID
MONDO_0009282
Q200779 (Deleted Item)
1 reference
stated in
Disease Ontology
retrieved
29 November 2020
Disease Ontology ID
DOID:0060358
Q5572455 (Deleted Item)
0 references
Disease Ontology ID
DOID:0060358
1 reference
stated in
Disease Ontology
retrieved
29 November 2020
Disease Ontology ID
DOID:0060358
instance of
Q42303753 (Deleted Item)
1 reference
reference URL
https://ddrare.nibiohn.go.jp/
retrieved
17 May 2019
Q112193867 (Deleted Item)
0 references
UMLS CUI
C3278154
mapping relation type
Q39893184 (Deleted Item)
1 reference
stated in
Q55345445 (Deleted Item)
retrieved
28 July 2018
Mondo ID
MONDO_0009282
C2931346
mapping relation type
Q39893184 (Deleted Item)
1 reference
stated in
Q55345445 (Deleted Item)
retrieved
28 July 2018
Mondo ID
MONDO_0009282
C3278156
mapping relation type
Q39893184 (Deleted Item)
1 reference
stated in
Q55345445 (Deleted Item)
retrieved
28 July 2018
Mondo ID
MONDO_0009282
C3278155
mapping relation type
Q39893184 (Deleted Item)
1 reference
stated in
Q55345445 (Deleted Item)
retrieved
28 July 2018
Mondo ID
MONDO_0009282
C1856403
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0060358
C0268596
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0060358
C1856401
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0060358
C1856405
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0060358
Orphanet ID
26791
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0060358
ICD-10-CM
E71.313
2 references
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0060358
stated in
Q55345445 (Deleted Item)
retrieved
28 July 2018
Mondo ID
MONDO_0009282
E71.3
1 reference
stated in
Q55345445 (Deleted Item)
retrieved
28 July 2018
Mondo ID
MONDO_0009282
MeSH descriptor ID
D054069
subject named as
Multiple Acyl Coenzyme A Dehydrogenase Deficiency
1 reference
stated in
Q55345445 (Deleted Item)
retrieved
28 July 2018
Mondo ID
MONDO_0009282
MeSH tree code
C16.320.565.100.614
0 references
C18.452.648.100.614
0 references
C18.452.660.612
0 references
health specialty
Q1071953 (Deleted Item)
0 references
endocrinology
0 references
genetic association
Q17917640 (Deleted Item)
2 references
stated in
Q905695 (Deleted Item)
UniProt protein ID
P38117
retrieved
13 August 2019
stated in
Q113138000 (Deleted Item)
retrieved
24 August 2023
reference URL
https://platform.opentargets.org/evidence/ENSG00000105379/MONDO_0009282
based on heuristic
Q121819027 (Deleted Item)
Microsoft Academic ID
2776200808
0 references
GARD rare disease ID
6523
0 references
PatientsLikeMe condition ID
glutaric-acidemia-type-ii
0 references
WikiProjectMed ID
Glutaric acidemia type 2
0 references
Mondo ID
MONDO_0009282
0 references
 
Retrieved from "https://rightwiki.org/index.php?title=Item:Q1403045&oldid=22045536"