01
Diseases
Ichthyosiform Erythroderma, Congenital
ichthyosiform erythroderma, congenital
- 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
- Ichthyosiform Erythroderma, Congenital
- Standard Disease Name
- ichthyosiform erythroderma, congenital
- MeSH Tree
- No data
- ICD-10
- No data
Identifiers
- DO ID
- No data
- MeSH ID
- D016113
- OMIM ID
- MTHU007979
- UMLS ID
- C0079583
- HPO ID
- No data
Description and Extensions
- Description
- MSH2017_2016_08_12:Designation for several severe forms of ichthyosis, present at birth, that are characterized by hyperkeratotic scaling. Infants may be born encased in a collodion membrane which begins shedding within 24 hours. This is followed in about two weeks by persistent generalized scaling. The forms include bullous (HYPERKERATOSIS, EPIDERMOLYTIC), non-bullous (ICHTHYOSIS, LAMELLAR), wet type, and dry type.|HPO2016_07_04:An ichthyosiform abnormality of the skin with congenital onset. [HPO:probinson]
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Candidate Herbs
target disease -> ingredient target -> herb ingredient8 Herbs