cataract, alopecia, sclerodactyly

Preferred Label : cataract, alopecia, sclerodactyly;

MeSH synonym : cataract, alopecia, sclerodactyly syndrome; Cataract-Alopecia-Sclerodactyly syndrome;

Details

Origin ID

C535336;

UMLS CUI

C1859316;

Automatic exact mappings (from CISMeF team)
- Autosomal recessive palmoplantar keratoderma and congenital alopecia [ICD-11 More detail]
- palmoplantar keratoderma and congenital alopecia 2 [DO Concept]
Currated CISMeF NLP mapping
- Autosomal recessive palmoplantar keratoderma and congenital alopecia [ORDO Disease]
- Autosomal recessive palmoplantar keratoderma and congenital alopecia syndrome (disorder) [SNOMED CT concept]
- Cataract - alopecia - sclerodactyly [ICD-11 More detail]
- Palmoplantar keratoderma and congenital alopecia 2 [OMIM Phenotype]
DO Cross reference
- palmoplantar keratoderma and congenital alopecia 2 [DO Concept]
MeSH term(s) associated for indexing
- alopecia [MeSH Descriptor]
- cataract [MeSH Descriptor]
- scleroderma, localized [MeSH Descriptor]
ORDO relation(s)
- Autosomal recessive palmoplantar keratoderma and congenital alopecia [ORDO Disease]
Record concept(s)
- Cataract, alopecia, sclerodactyly [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal recessive palmoplantar keratoderma and congenital alopecia [ORDO Disease]
- Palmoplantar keratoderma and congenital alopecia 2 [OMIM Phenotype]
- palmoplantar keratoderma and congenital alopecia 2 [DO Concept]

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