OMOP Concept 36714028

Autosomal recessive palmoplantar keratoderma and congenital alopecia syndrome

StandardConditionSNOMED719104003Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
OMOP concepts

Concept Lookup Tool

Search 11M+ concepts across SNOMED, RxNorm, ICD-10 & LOINC.

Source codes that map to this concept

1 source code normalizes to Autosomal recessive palmoplantar keratoderma and congenital alopecia syndrome via the OMOP "Maps to" relationship.

Synonyms

Alternative names recorded for Autosomal recessive palmoplantar keratoderma and congenital alopecia syndrome across source vocabularies.

  • Autosomal recessive palmoplantar keratoderma and congenital alopecia syndrome (disorder)
  • Autosomal recessive palmoplantar keratoderma and congenital alopecia Wallis type
  • síndrome de queratodermia palmoplantar autosómica recesiva y alopecia congénita
  • síndrome de queratodermia palmoplantar autosómica recesiva y alopecia congénita (trastorno)

Where it sits in the hierarchy

Ordered by distance - 1 is a direct parent or child.

Get this concept via the API

Resolve Autosomal recessive palmoplantar keratoderma and congenital alopecia syndrome - and every code that maps to it - over HTTPS, against the current vocabulary release. No downloads, no local database.

curl "https://api.omophub.com/v1/concepts/36714028?include_relationships=true" \
  -H "Authorization: Bearer $OMOPHUB_API_KEY"
Get your free API key3,000 calls/month free · no credit card