mitochondrial disease
spontaneously occuring or inherited disorder that involves mitochondrial dysfunction
External resources
| ଫ୍ରୀବେସ ସୂଚକ | |
| SNOMED CT ID | |
| MeSH descriptor ID | |
| Encyclopædia Britannica Online ID | science/mitochondrial-disorder subject named as: mitochondrial disease author name string: Kara Rogers |
| YSO ID | |
| PatientsLikeMe condition ID | |
| KEGG ID | |
| DiseasesDB | |
| Orphanet ID | |
| 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 |
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
on focus list of Wikimedia project
exact match
କମନ୍ସ ଶ୍ରେଣୀ
Mitochondrial diseases
ବିଷୟର ମୁଖ୍ୟ ଶ୍ରେଣୀ
Category:Mitochondrial diseases
ଆଧାର
- ↑ Freebase Data Dumps, ୨୮ ଅକ୍ଟୋବର 2013
- ↑ ୨.୦ ୨.୧ ୨.୨ ୨.୩ ୨.୪ ୨.୫ Monarch Disease Ontology release 2018-06-29, ୨୮ ଜୁଲାଇ 2018, MONDO_0004069
- ↑ YSO-Wikidata mapping project, ୨୭ ଡିସେମ୍ବର 2021
- ↑ ୪.୦ ୪.୧ Disease Ontology, ୨୮ ଅଗଷ୍ଟ 2019, DOID:0080013
- ↑ ୫.୦ ୫.୧ ୫.୨ Disease Ontology, ୧୫ ମଇ 2019, DOID:700
- ↑ BabelNet
- ↑ ୭.୦ ୭.୧ OpenAlex, ୨୬ ଜାନୁଆରୀ 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
- ↑ ୮.୦ ୮.୧ https://ddrare.nibiohn.go.jp/, ୧୭ ମଇ 2019
- ↑ ୯.୦ ୯.୧ Disease Ontology, ୩୦ ନଭେମ୍ବର 2020, DOID:700
- ↑ Identifiers.org, https://registry.identifiers.org/registry/doid