01
- Entity Type
- Diseases
- Relation Groups
- 3
- Relation Preview
- 24
Basic Information
Grouped by core information, identifiers, and descriptions.
Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.
Core Information
- Disease Name
- Anaplasia
- Standard Disease Name
- anaplasia
- MeSH Tree
- No data
- ICD-10
- No data
Identifiers
- DO ID
- No data
- MeSH ID
- C536614
- OMIM ID
- 208100
- UMLS ID
- C1859721
- HPO ID
- No data
Description and Extensions
- Description
- SNOMEDCT_US_2016_09_01:A form of arthrogryposis multiplex congenital characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is caused by neurogenic muscular atrophy.|SNOMEDCT_US_2016_09_01:A form of arthrogryposis multiplex congenital characterised by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is caused by neurogenic muscular atrophy.
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Candidate Ingredients
target disease -> ingredient target8 Ingredients
02
(−)-Alloaromadendrene
No data
03
()-2-Carene
No data
04
()-Aromadendrene
No data
05
06
()-Beta-Pinene
No data
07
()-Cuparene
No data
08
()-Ledene
No data