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43327007: Acantholysis (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
72276015 Acantholysis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
780326013 Acantholysis (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Acantholysis Is a Lysis false Inferred relationship Some
Acantholysis Is a Lysis (morphologic abnormality) true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Familial acantholysis Associated morphology True Acantholysis Inferred relationship Some 1
Persistent acantholytic dermatosis of Fawcett and Miller Associated morphology False Acantholysis Inferred relationship Some 1
Transient acantholytic dermatosis Associated morphology False Acantholysis Inferred relationship Some 1
Transient acantholytic dermatosis Associated morphology True Acantholysis Inferred relationship Some 1
Persistent acantholytic dermatosis of Fawcett and Miller Associated morphology True Acantholysis Inferred relationship Some 1
Benign acantholytic dermatosis of vulva (disorder) Associated morphology True Acantholysis Inferred relationship Some 1
A rare, genetic, developmental defect during embryogenesis syndrome characterized by generalized keratosis follicularis, severe proportionate dwarfism and cerebral atrophy. Alopecia (of scalp, eyebrows and eyelashes) and microcephaly are additionally observed features. Intellectual disability, inguinal hernia and epilepsy may also be associated. There have been no further descriptions in the literature since 1974. Associated morphology True Acantholysis Inferred relationship Some 4
Relapsing linear acantholytic dermatosis (disorder) Associated morphology False Acantholysis Inferred relationship Some 2
Hereditary acantholytic dermatosis Associated morphology True Acantholysis Inferred relationship Some 1
Darier disease Associated morphology True Acantholysis Inferred relationship Some 1
Acquired acantholytic dermatosis (disorder) Associated morphology True Acantholysis Inferred relationship Some 1
Nail dystrophy due to Darier's disease (disorder) Associated morphology False Acantholysis Inferred relationship Some 1
Acral Darier's disease (disorder) Associated morphology True Acantholysis Inferred relationship Some 1
Palmar pitting due to Darier disease Associated morphology True Acantholysis Inferred relationship Some 1
Acrokeratosis verruciformis of Darier disease (disorder) Associated morphology True Acantholysis Inferred relationship Some 1
Flexural Darier's disease (disorder) Associated morphology True Acantholysis Inferred relationship Some 1
Hypertrophic Darier's disease (disorder) Associated morphology True Acantholysis Inferred relationship Some 1
Linear/nevoid/zosteriform Darier's disease (disorder) Associated morphology True Acantholysis Inferred relationship Some 1
Nail dystrophy due to Darier's disease (disorder) Associated morphology True Acantholysis Inferred relationship Some 2
Eosinophilic spongiosis (prebullous pemphigus) (disorder) Associated morphology False Acantholysis Inferred relationship Some 1
A rare superficial pemphigus disease characterized by severe intractable pruritus with erythematous or urticarial plaques and sometimes vesicles organized in a herpetiform pattern. Mucosae are generally spared. Eosinophilia in peripheral blood and low titers of circulating autoantibodies are observed in many cases. Histology can show an aspect of either pemphigus (superficial or deep), or an intraepidermal infiltrate rich in eosinophils (eosinophilic spongiosis). Associated morphology False Acantholysis Inferred relationship Some 1
Pemphigus vulgaris Associated morphology True Acantholysis Inferred relationship Some 1
Drug-induced pemphigus Associated morphology False Acantholysis Inferred relationship Some 1
Drug-induced pemphigus vulgaris (disorder) Associated morphology False Acantholysis Inferred relationship Some 1
IgA pemphigus Associated morphology False Acantholysis Inferred relationship Some 1
Pemphigus paraneoplastica (disorder) Associated morphology False Acantholysis Inferred relationship Some 1
Pemphigus vegetans Associated morphology True Acantholysis Inferred relationship Some 1
Pemphigus foliaceus Associated morphology True Acantholysis Inferred relationship Some 2
Pemphigus Associated morphology False Acantholysis Inferred relationship Some 1
Pemphigus vegetans of Neumann type Associated morphology True Acantholysis Inferred relationship Some 1
Familial benign pemphigus Associated morphology True Acantholysis Inferred relationship Some 2
Pemphigus neonatorum Associated morphology False Acantholysis Inferred relationship Some 1
Pemphigus of vulva (disorder) Associated morphology True Acantholysis Inferred relationship Some 2
Pemphigus vulgaris of gingival mucous membrane (disorder) Associated morphology True Acantholysis Inferred relationship Some 2
Oral pemphigus vulgaris Associated morphology True Acantholysis Inferred relationship Some 2
pemphigus foliacé brésilien Associated morphology False Acantholysis Inferred relationship Some 2
Pemphigus erythematosus Associated morphology True Acantholysis Inferred relationship Some 2
Drug-induced pemphigus foliaceus (disorder) Associated morphology True Acantholysis Inferred relationship Some 2
Drug-induced pemphigus vulgaris (disorder) Associated morphology True Acantholysis Inferred relationship Some 2
Eosinophilic spongiosis (prebullous pemphigus) (disorder) Associated morphology True Acantholysis Inferred relationship Some 2
Drug-induced pemphigus Associated morphology True Acantholysis Inferred relationship Some 2
Pemphigus Associated morphology True Acantholysis Inferred relationship Some 2
IgA pemphigus Associated morphology True Acantholysis Inferred relationship Some 2
A rare superficial pemphigus disease characterized by severe intractable pruritus with erythematous or urticarial plaques and sometimes vesicles organized in a herpetiform pattern. Mucosae are generally spared. Eosinophilia in peripheral blood and low titers of circulating autoantibodies are observed in many cases. Histology can show an aspect of either pemphigus (superficial or deep), or an intraepidermal infiltrate rich in eosinophils (eosinophilic spongiosis). Associated morphology True Acantholysis Inferred relationship Some 2
Pemphigus paraneoplastica (disorder) Associated morphology True Acantholysis Inferred relationship Some 2
Pemphigus neonatorum Associated morphology True Acantholysis Inferred relationship Some 2
Acantholysis of skin (disorder) Associated morphology True Acantholysis Inferred relationship Some 1
A rare autoimmune bullous skin disease characterized by the formation of subcorneal blisters mediated by autoantibodies against desmoglein 1, affecting predominantly seborrheic areas such as the head, neck, and upper trunk, but without any mucosal involvement. The lesions may be worsened by exposure to UV light and typically progress over weeks or months. The disease frequently occurs in children and young adults and is endemic to rural areas of Brazil and other countries in South America, as well as North Africa. Associated morphology True Acantholysis Inferred relationship Some 2

This concept is not in any reference sets

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