Scalp-ear-nipple syndrome

Preferred Label : Scalp-ear-nipple syndrome;

ICD-11 definition : Scalp-ear-nipple syndrome is characterised by the following triad: areas of hairless raw skin over the scalp (present at birth and healing during childhood), prominent, hypoplastic ears with almost absent pinnae, and bilateral amastia.;

Details

Origin ID

88843032;

UMLS CUI

C1867020;

Automatic exact mappings (from CISMeF team)
- scalp-ear-nipple syndrome [DO Concept]
Currated CISMeF NLP mapping
- Scalp ear nipple syndrome [MeSH concept]
- Scalp, ear, nipple syndrome (disorder) [SNOMED CT concept]
- Scalp-ear-nipple syndrome [OMIM Phenotype]
- Scalp-ear-nipple syndrome [ORDO Disease]
- scalp ear nipple syndrome [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Scalp ear nipple syndrome [MeSH concept]
- Scalp, ear, nipple syndrome (disorder) [SNOMED CT concept]
- Scalp-ear-nipple syndrome [OMIM Phenotype]
- Scalp-ear-nipple syndrome [ORDO Disease]
- scalp ear nipple syndrome [MeSH Supplementary Concept]
- scalp-ear-nipple syndrome [DO Concept]

Keyword's position in hierarchy(ies) :

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