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772126000: Poikiloderma with neutropenia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3717147017 Poikiloderma with neutropenia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3717148010 Poikiloderma with neutropenia Clericuzio type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3717150019 Poikiloderma with neutropenia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3716696016 A disorder of the skin and immune system with initial manifestation of a bumpy skin rash usually between the ages of 6 and 12 months, gradually spreading from the arms and legs to the torso and face. At about age 2, the rash fades leaving hyperpigmentation and hypopigmentation and telangiectases, this combination is known as poikiloderma. Palmoplantar keratoderma, calcinosis cutis, skin ulcers, pachyonychia, fragile teeth and low bone density may also be present. Chronic neutropenia is present resulting in recurrent sinus infections and pneumonia, especially in the first few years of life. Caused by mutations in the USB1 gene. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4218241000052111 poikiloderma med neutropeni sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Poikiloderma with neutropenia Finding site Skin structure true Inferred relationship Some 2
Poikiloderma with neutropenia Associated morphology Poikiloderma true Inferred relationship Some 2
Poikiloderma with neutropenia Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Poikiloderma with neutropenia Is a Chronic disease of skin true Inferred relationship Some
Poikiloderma with neutropenia Is a Neutropenic disorder true Inferred relationship Some
Poikiloderma with neutropenia Is a Hereditary disorder of the integument true Inferred relationship Some
Poikiloderma with neutropenia Clinical course Chronic true Inferred relationship Some 3
Poikiloderma with neutropenia Interprets Neutrophil count true Inferred relationship Some 1
Poikiloderma with neutropenia Is a Hereditary white blood cell disorder (disorder) true Inferred relationship Some
Poikiloderma with neutropenia Is a Poikiloderma (disorder) true Inferred relationship Some
Poikiloderma with neutropenia Has interpretation Below reference range true Inferred relationship Some 1
Poikiloderma with neutropenia Is a Chronic disease of immune function (disorder) true Inferred relationship Some
Poikiloderma with neutropenia Pathological process (attribute) Abnormal immune process (qualifier value) true Inferred relationship Some 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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