burnett schwartz berberian syndrome

Preferred Label : burnett schwartz berberian syndrome;

MeSH note : Keratosis pilaris affecting the follicles of the eyebrow hairs;

CISMeF synonym : amelogenesis imperfecta, hypoplastic/hypomaturation, X-linked 2; atrophodermia reticulata; keratosis pilaris;

MeSH synonym : ulerythema ophryogenes; ulerythema ophryogenes with multiple congenital anomalies; keratosis pilaris atrophicans facies; folliculitis ulerythematosa; honeycomb atrophy; ulerythema ophryogenesis; atrophodermia vermiculata;

Related MeSH term : Folliculitis ulerythematosa reticulata; Atrophodermia Reticulata Symmetrica Faciei;

Details

Origin ID

C537412;

UMLS CUI

C0263428;

Automatic exact mappings (from CISMeF team)
- Amelogenesis imperfecta, hypoplastic/hypomaturation, X-linked 2 [OMIM Phenotype]
- Atrophoderma vermiculata [MedDRA LLT]
- Atrophoderma vermiculata [ORDO Disease]
- Atrophoderma vermiculata [OMIM Phenotype]
- Atrophoderma vermiculatum [PASCAL descriptor]
- Atrophoderma vermiculatum [ICD-11 More detail]
- Atrophoderma vermiculatum (disorder) [SNOMED CT concept]
- Atrophodermia vermiculata [HPO term]
- Folliculitis ulerythematosa reticulata [MedDRA LLT]
- Folliculitis ulerythematosa reticulata [ICD-10 Sub-category (who)]
- Keratosis Pilaris [NCIt concept]
- Keratosis pilaris [ICD-11 Category]
- Keratosis pilaris [HPO term]
- Keratosis pilaris [MedDRA Preferred Term]
- Keratosis pilaris (disorder) [SNOMED CT concept]
- Keratosis pilaris atrophicans [OMIM Phenotype]
- Pilaris keratosis [PASCAL descriptor]
- Ulerythema ophryogenes [ICD-11 More detail]
- Ulerythema ophryogenes (disorder) [SNOMED CT concept]
- Ulerythema ophryogenesis [ORDO Disease]
- X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 [DO Concept]
- atrophoderma vermiculatum [SNOMED Notion]
- folliculitis ulerythematosa reticulata [SNOMED Notion]
- keratosis pilaris [SNOMED Notion]
CISMeF manual mappings
- Keratosis pilaris atrophicans (disorder) [SNOMED CT concept]
HPO term
- Atrophodermia vermiculata [HPO term]
MeSH term(s) associated for indexing
- abnormalities, multiple [MeSH Descriptor]
- darier disease [MeSH Descriptor]
- eyebrows [MeSH Descriptor]
Record concept(s)
- Amelogenesis imperfecta, hypoplastic-hypomaturation, X-linked 2 [MeSH concept]
- atrophodermia reticulata [MeSH concept]
- burnett schwartz berberian syndrome [MeSH concept]
- keratosis pilaris [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Atrophodermia vermiculata [HPO term]
- Keratosis pilaris atrophicans [ORDO Disease]
- Keratosis pilaris atrophicans [OMIM Phenotype]
- Keratosis pilaris atrophicans [MedDRA Preferred Term]
- Keratosis pilaris atrophicans (disorder) [SNOMED CT concept]
- Ulerythema ophryogenes (disorder) [SNOMED CT concept]
- ulerythema of eyebrows [SNOMED Notion]

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