Atrophoderma vermiculata

Preferred Label : Atrophoderma vermiculata;

Symbol : AVA;

CISMeF acronym : AVA;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Atrophodermia reticulata symmetrica faciei; Folliculitis ulerythematosa reticulata; Atrophodermia vermiculata; Honeycomb atrophy;

Description : Atrophoderma vermiculata, a form of keratosis pilaris atrophicans, typically presents in childhood with erythema and follicular keratotic papules that slowly progress to characteristic atrophy, which has been described as worm-eaten, reticular, or honeycomb, and occurs on the cheeks, preauricular area, and forehead. More rarely, the atrophy may extend to the upper lip, helices, ear lobes, and, in some cases, the limbs. The degree of inflammation, the presence of milia, and the extent of follicular plugs are variable (summary by Luria and Conologue, 2009).;

Inheritance : Autosomal dominant;

Prefixed ID : %209700;

Details

Origin ID

209700;

UMLS CUI

C0263429;

Automatic exact mappings (from CISMeF team)
- Amsacrine/Azacitidine/Etoposide Regimen [NCIt concept]
- Arteriovenous angioma (disorder) [SNOMED CT concept]
- Avar Language [NCIt concept]
- burnett schwartz berberian syndrome [MeSH Supplementary Concept]
Currated CISMeF NLP mapping
- Atrophoderma vermiculata [MedDRA LLT]
- Atrophoderma vermiculata [ORDO Disease]
- 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]
- atrophoderma vermiculata [DO Concept]
- atrophoderma vermiculatum [SNOMED Notion]
- folliculitis ulerythematosa reticulata [SNOMED Notion]
DO Cross reference
- atrophoderma vermiculata [DO Concept]
False automatic mappings
- atrophodermia reticulata [MeSH concept]
HPO term(s)
- Abnormality of the cardiovascular system [HPO term]
- Abnormality of the face [HPO term]
- Abnormality of the skin [HPO term]
- Atrophodermia vermiculata [HPO term]
- Autosomal dominant inheritance [HPO term]
- Autosomal recessive inheritance [HPO term]
- Leukonychia [HPO term]
- Milia [HPO term]
ORDO concept(s)
- Atrophoderma vermiculata [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Atrophoderma vermiculata [ORDO Disease]
- Atrophoderma vermiculata [MedDRA LLT]
- Atrophoderma vermiculatum (disorder) [SNOMED CT concept]
- Atrophodermia vermiculata [HPO term]
- Folliculitis ulerythematosa reticulata [ICD-10 Sub-category (who)]
- Folliculitis ulerythematosa reticulata [ICD-10 Sub-category]
- Folliculitis ulerythematosa reticulata [MedDRA LLT]
- atrophoderma vermiculatum [SNOMED Notion]
- atrophodermia reticulata [MeSH concept]
- folliculitis ulerythematosa reticulata [SNOMED Notion]

Keyword's position in hierarchy(ies) :

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