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70114006: Poikiloderma (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
116442013 Poikiloderma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
810135019 Poikiloderma (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
Poikiloderma Is a Atrophy true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary acrokeratotic poikiloderma of Weary Associated morphology False Poikiloderma Inferred relationship Some 1
A rare inherited epidermolysis bullosa (EB) characterized by skin fragility and blistering at birth followed by development of photosensitivity and progressive poikilodermatous skin changes. Associated morphology False Poikiloderma Inferred relationship Some 1
Diffuse and macular atrophic dermatosis of Stevanovic Associated morphology False Poikiloderma Inferred relationship Some 1
Acquired poikiloderma (disorder) Associated morphology False Poikiloderma Inferred relationship Some 1
Poikiloderma of Civatte Associated morphology True Poikiloderma Inferred relationship Some 2
Rothmund-Thomson syndrome Associated morphology True Poikiloderma Inferred relationship Some 1
Poikiloderma caused by cold injury Associated morphology False Poikiloderma Inferred relationship Some 1
Poikiloderma due to heat of infrared radiation therapy (disorder) Associated morphology False Poikiloderma Inferred relationship Some 1
Poikiloderma caused by photodynamic agent (disorder) Associated morphology True Poikiloderma Inferred relationship Some 1
Poikiloderma due to connective tissue disease (disorder) Associated morphology False Poikiloderma Inferred relationship Some 1
Poikiloderma due to lichen planus (disorder) Associated morphology False Poikiloderma Inferred relationship Some 1
Poikiloderma (disorder) Associated morphology False Poikiloderma Inferred relationship Some 1
poïkilodermie avec syndrome génétique ou congénital Associated morphology False Poikiloderma Inferred relationship Some 2
Poikiloderma due to lupus erythematosus Associated morphology False Poikiloderma Inferred relationship Some 1
Poikiloderma due to scleroderma Associated morphology False Poikiloderma Inferred relationship Some 1
Telangiectasia caused by ionizing radiation (disorder) Associated morphology False Poikiloderma Inferred relationship Some 3
Hereditary sclerosing poikiloderma of Weary (disorder) Associated morphology False Poikiloderma Inferred relationship Some 2
Poikilodermatous mycosis fungoides (disorder) Associated morphology True Poikiloderma Inferred relationship Some 2
poïkilodermie avec syndrome génétique ou congénital Associated morphology False Poikiloderma Inferred relationship Some 2
Poikiloderma due to lichen planus (disorder) Associated morphology True Poikiloderma Inferred relationship Some 1
Poikiloderma (disorder) Associated morphology True Poikiloderma Inferred relationship Some 1
Acquired poikiloderma (disorder) Associated morphology True Poikiloderma Inferred relationship Some 1
Poikiloderma due to lupus erythematosus Associated morphology True Poikiloderma Inferred relationship Some 1
Poikiloderma due to heat of infrared radiation therapy (disorder) Associated morphology True Poikiloderma Inferred relationship Some 1
Hereditary acrokeratotic poikiloderma of Weary Associated morphology True Poikiloderma Inferred relationship Some 1
Hereditary sclerosing poikiloderma of Weary (disorder) Associated morphology True Poikiloderma Inferred relationship Some 2
Diffuse and macular atrophic dermatosis of Stevanovic Associated morphology True Poikiloderma Inferred relationship Some 1
Poikiloderma due to connective tissue disease (disorder) Associated morphology True Poikiloderma Inferred relationship Some 1
Poikiloderma caused by cold injury Associated morphology True Poikiloderma Inferred relationship Some 1
Poikiloderma due to scleroderma Associated morphology True Poikiloderma Inferred relationship Some 1
A rare inherited epidermolysis bullosa (EB) characterized by skin fragility and blistering at birth followed by development of photosensitivity and progressive poikilodermatous skin changes. Associated morphology True Poikiloderma Inferred relationship Some 1
Poikiloderma caused by ionizing radiation Associated morphology True Poikiloderma Inferred relationship Some 1
Hereditary sclerosing poikiloderma Associated morphology True Poikiloderma Inferred relationship Some 1
Hereditary fibrosing poikiloderma-tendon contractures-myopathy-pulmonary fibrosis syndrome is a rare, genetic, hereditary poikiloderma syndrome characterized by early-onset poikiloderma (mainly on the face), hypotrichosis, hypohidrosis, muscle and tendon contractures with varus foot deformity, progressive proximal and distal muscle weakness in all extremities, and progressive pulmonary fibrosis. Mild lymphedema of the extremities, growth retardation, liver impairment, exocrine pancreatic insufficiency and hematologic abnormalities are additional variable features. Associated morphology True Poikiloderma Inferred relationship Some 3
PARC syndrome is a rare genetic developmental defect during embryogenesis syndrome characterized by the association of congenital poikiloderma (P), generalized alopecia (A), retrognathism (R) and cleft palate (C). There have been no further descriptions in the literature since 1990. Associated morphology True Poikiloderma Inferred relationship Some 4
Poikiloderma with neutropenia is a rare, genetic hereditary poikiloderma disorder characterized by early-onset poikiloderma (which typically begins in the extremities, progresses centripetally and eventually involves the trunk, face and ears) associated with chronic neutropenia, recurrent infections, pachyonychia and palmoplantar keratoderma. Growth and/or developmental delay and hepato- and/or splenomegaly are additional reported features. Associated morphology True Poikiloderma Inferred relationship Some 2
Poikiloderma caused by photodynamic agent (disorder) Associated morphology False Poikiloderma Inferred relationship Some 3
Poikilodermatomyositis Associated morphology True Poikiloderma Inferred relationship Some 3
Rothmund Thomson syndrome type 1 (disorder) Associated morphology True Poikiloderma Inferred relationship Some 1
Rothmund Thomson syndrome type 2 Associated morphology True Poikiloderma Inferred relationship Some 1
Poikiloderma due to and following radiotherapy (disorder) Associated morphology True Poikiloderma Inferred relationship Some 1

This concept is not in any reference sets

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