FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

402335001: Familial psoriasis (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1770259012 Familial psoriasis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1781492017 Familial psoriasis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
305571000077114 psoriasis familial fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


3 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial psoriasis (disorder) Is a Psoriasis true Inferred relationship Some
Familial psoriasis (disorder) Finding site Skin structure true Inferred relationship Some 1
Familial psoriasis (disorder) Has definitional manifestation Abnormal keratinization false Inferred relationship Some
Familial psoriasis (disorder) Due to réaction d'hypersensibilité immunitaire false Inferred relationship Some
Familial psoriasis (disorder) Due to A pathological process initiated by exposure to a defined stimulus at a dose tolerated by normal persons. It may be the manifestation of a disposition to hypersensitivity. false Inferred relationship Some
Familial psoriasis (disorder) Pathological process (attribute) An immune or non-immune mediated pathological process that represents the underlying mechanism of hypersensitivity conditions. true Inferred relationship Some 2
Familial psoriasis (disorder) Pathological process (attribute) Abnormal immune process (qualifier value) false Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group
Familial psoriasis with affected first degree relative (disorder) Is a True Familial psoriasis (disorder) Inferred relationship Some
Familial psoriasis without affected first degree relative (disorder) Is a True Familial psoriasis (disorder) Inferred relationship Some
A rare, X-linked syndromic intellectual disability disorder characterized by severe intellectual disability, psychomotor developmental delay, generalized seizures, and psoriasis. Mild craniofacial dysmorphism, such as hypertelorism, broad nasal bridge, anteverted nares, macrostomia, highly arched palate and large ears, is also associated. There have been no further descriptions in the literature since 1988. Is a True Familial psoriasis (disorder) Inferred relationship Some

This concept is not in any reference sets

Back to Start