DiseaseID 25957
母系遗传性心肌病与听力丧失
Maternally-Inherited Cardiomyopathy And Hearing Loss
Maternally inherited cardiomyopathy and hearing loss is a mitochondrial disease described in two unrelated families to date that has a heterogeneous clinical presentation characterized by the associat
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
Click a node to open it in a new tab
Disease: 1Symptom: 9Target: 2Links: 11
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 25957
- Core Entity Id
- 118525
- Source Entity Count
- 1
- Preferred Name
- Maternally-Inherited Cardiomyopathy And Hearing Loss
- Name Cn
- 母系遗传性心肌病与听力丧失
- Name Pinyin
- Mu Xi Yi Chuan Xing Xin Ji Bing Yu Ting Li Sang Shi
- Name En
- Maternally-Inherited Cardiomyopathy And Hearing Loss
- Name Latin
- Bilingual Status
- complete
- Disease Type
- Umls Disease Type
- Disgenet Type
- Mesh Class
- Do Class
- Hpo Class
- Mesh Class Name
- Hpo Class Name
- Do Class Name
- Disease Definition
- Maternally inherited cardiomyopathy and hearing loss is a mitochondrial disease described in two unrelated families to date that has a heterogeneous clinical presentation characterized by the associat
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Maternally-Inherited Cardiomyopathy And Hearing Loss
Role
preferred
Source
SymMap_v2
Preferred
Yes
Cross References
Trusted external identifiers retained for this final record.
Sym Map
SMDE01265
Orphanet
1349
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Disease Definition
Maternally inherited cardiomyopathy and hearing loss is a mitochondrial disease described in two unrelated families to date that has a heterogeneous clinical presentation characterized by the associat