OMOP Concept 44784143

Schöpf-Schulz-Passarge syndrome

StandardConditionSNOMED700062000Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2014
Valid to
31 Dec 2099
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Source codes that map to this concept

1 source code normalizes to Schöpf-Schulz-Passarge syndrome via the OMOP "Maps to" relationship.

VocabularyCodeNameType
MeSHC565607Schopf-Schulz-Passarge SyndromeNon-standard

Synonyms

Alternative names recorded for Schöpf-Schulz-Passarge syndrome across source vocabularies.

  • Eccrine tumors ectodermal dysplasia
  • Eccrine tumours ectodermal dysplasia
  • Keratosis palmoplantaris, cystic eyelids, hypodontia, hypotrichosis syndrome
  • Palmoplantar hyperkeratosis, cystic eyelids, hypodontia, hypotrichosis syndrome
  • Palmoplantar keratoderma, cystic eyelids, hypodontia, hypotrichosis syndrome
  • Schöpf Schulz Passarge syndrome
  • Schöpf-Schulz-Passarge syndrome (disorder)
  • síndrome de queratosis palmoplantar, párpados quísticos, hipodoncia e hipotricosis
  • síndrome de Schöpf-Schulz-Passarge
  • síndrome de Schöpf-Schulz-Passarge (trastorno)
  • SSPS - Schöpf Schulz Passarge syndrome
  • SSSP - síndrome de Schöpf Schulz Passarge
  • tumores ecrinos y displasia ectodérmica

Where it sits in the hierarchy

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

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