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mitochondrial disease

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spontaneously occuring or inherited disorder that involves mitochondrial dysfunction

External resources

ଫ୍ରୀବେସ ସୂଚକ
SNOMED CT ID
MeSH descriptor ID
D028361[୨]

subject named as: Mitochondrial Diseases

mapping relation type: exact match

Encyclopædia Britannica Online ID
science/mitochondrial-disorder

subject named as: mitochondrial disease

author name string: Kara Rogers

YSO ID
20681[୩]

subject named as: mitokondriotaudit, mitokondriesjukdomar, mitochondrial diseases

PatientsLikeMe condition ID
KEGG ID
DiseasesDB
Orphanet ID
68380[୨]

mapping relation type: exact match

Disease Ontology ID
WikiProjectMed ID
MeSH tree code
JSTOR topic ID
WikiSkripta article ID
UMLS CUI
BabelNet ID
GARD rare disease ID
ICD-10-CM
Microsoft Academic ID
OpenAlex ID
ICD-୯
NL CR AUT ID
ph893660

subject named as: mitochondrialní onemocnění

Mondo ID

ଦୃଷ୍ଟାନ୍ତ

ଭୃଣ ତିଆରି ସମୟରେ ବିକାଶ ତୃଟି[୨]
ଅସାଧ୍ୟ/କ୍ୱଚିତ ରୋଗ[୮]
class of disease

ଏହାର ମୁଖ୍ୟଶ୍ରେଣୀ

inherited metabolic disorder[୯]
mtDNA transmission
developmental anomaly of metabolic origin[୨]
inborn disorder of energy metabolism[୨]

ଚିକିତ୍ସା ଶ୍ରେଣୀ

endocrinology

mode of inheritance

mtDNA transmission

external data available at URL

କମନ୍ସ ଶ୍ରେଣୀ

Mitochondrial diseases

ବିଷୟର ମୁଖ୍ୟ ଶ୍ରେଣୀ

Category:Mitochondrial diseases

ଆଧାର

  1. Freebase Data Dumps, ୨୮ ଅକ୍ଟୋବର 2013
  2. ୨.୦ ୨.୧ ୨.୨ ୨.୩ ୨.୪ ୨.୫ Monarch Disease Ontology release 2018-06-29, ୨୮ ଜୁଲାଇ 2018, MONDO_0004069
  3. YSO-Wikidata mapping project, ୨୭ ଡିସେମ୍ବର 2021
  4. ୪.୦ ୪.୧ Disease Ontology, ୨୮ ଅଗଷ୍ଟ 2019, DOID:0080013
  5. ୫.୦ ୫.୧ ୫.୨ Disease Ontology, ୧୫ ମଇ 2019, DOID:700
  6. BabelNet
  7. ୭.୦ ୭.୧ OpenAlex, ୨୬ ଜାନୁଆରୀ 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
  8. ୮.୦ ୮.୧ https://ddrare.nibiohn.go.jp/, ୧୭ ମଇ 2019
  9. ୯.୦ ୯.୧ Disease Ontology, ୩୦ ନଭେମ୍ବର 2020, DOID:700
  10. Identifiers.org, https://registry.identifiers.org/registry/doid