01
Diseases
Autosomal Dominant Palmoplantar Keratoderma And Congenital Alopecia
autosomal dominant palmoplantar keratoderma and congenital alopecia
- Entity Type
- Diseases
- Relation Groups
- 3
- Relation Preview
- 17
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
- Autosomal Dominant Palmoplantar Keratoderma And Congenital Alopecia
- Standard Disease Name
- autosomal dominant palmoplantar keratoderma and congenital alopecia
- MeSH Tree
- No data
- ICD-10
- Q82.8
Identifiers
- DO ID
- No data
- MeSH ID
- C537050
- OMIM ID
- 104100
- UMLS ID
- C1863093
- HPO ID
- No data
Description and Extensions
- Description
- Autosomal dominant palmoplantar keratoderma with congenital alopecia (PPK-CA) is a rare genetic skin disorder characterized by absence of scalp and body hair and palmoplantar keratoderma, without othe
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Candidate Ingredients
target disease -> ingredient target8 Ingredients
02
03
(-)-noradrenaline
No data
04
(?)-Secoisolariciresinol
No data
05
06
17-Beta-Estradiol
No data
07
08
18beta-glycyrrhetinic acid
No data