01
Diseases
Bulbo-Spinal Atrophy, X-Linked
bulbo-spinal atrophy, x-linked
- 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
- Bulbo-Spinal Atrophy, X-Linked
- Standard Disease Name
- bulbo-spinal atrophy, x-linked
- MeSH Tree
- No data
- ICD-10
- No data
Identifiers
- DO ID
- No data
- MeSH ID
- D055534
- OMIM ID
- 313200|313700
- UMLS ID
- C1839259
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_02D:A rare, slowly progressive degenerative disorder affecting males. It is caused by mutations in the androgen receptor (AR) gene. It is characterized by bulbar and limb muscle weakness and atrophy, and gynecomastia.|MSH2017_2016_08_12:An X-linked recessive form of spinal muscular atrophy. It is due to a mutation of the gene encoding the ANDROGEN RECEPTOR.
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Candidate Ingredients
target disease -> ingredient target8 Ingredients
02
()-Bornyl Acetate
No data
03
04
()-Cuparene
No data
05
06
(+)-(Z)-Methyl epijasmonate
No data
07
08
(+)-Anomalin
No data