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.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C565607 | Schopf-Schulz-Passarge Syndrome | Non-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.
Broader concepts
(125)Roll up to these when you need a wider cohort.
- 1Autosomal hereditary disorder
- 1Congenital anomaly in number of teeth
- 1Cyst of eyelid
- 1Developmental hereditary disorder
- 1Dystrophia unguium
- 1Ectodermal dysplasia with hair-tooth-nail defects
- 1Genetic disorder of nail
- 1Hereditary cancer-predisposing syndrome
- 1Hereditary diffuse palmoplantar keratoderma
- 1Hereditary disorder of the visual system
- 1Hereditary disorder of tooth
- 1Hypotrichosis
- 2Congenital anomaly of tooth
- 2Cyst of face
- 2Degenerative disorder of extremity
- 2Degenerative skin disorder
- 2Developmental disorder
- 2Digestive system hereditary disorder
- 2Disorder of hair growth
- 2Disorder of nail
- 2Ectodermal dysplasia with hair-nail defect
- 2Ectodermal dysplasia with hair-tooth defects
- 2Ectodermal dysplasia with tooth-nail defects
- 2Genetic disease
- 2Hereditary disease
Showing 25 of 125. Retrieve the full set via the API.
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