FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

763401009: Ichthyosis prematurity syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3642106015 Congenital ichthyosis type 4 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3642107012 Ichthyosis prematurity syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3642108019 Ichthyosis prematurity syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3642109010 A rare syndromic congenital ichthyosis with characteristics of premature birth in addition to thick caseous and desquamating epidermis, neonatal respiratory asphyxia and persistent eosinophilia. After the perinatal period, a spontaneous improvement in the health of affected patients is observed and skin features (vernix caseosa-like scale) evolve into a mild presentation of flat follicular hyperkeratosis with atopy. The disease is caused by mutation in the FATP4 (SLC27A4) gene. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Ichthyosis prematurity syndrome Is a Congenital ichthyosis of skin false Inferred relationship Some
Ichthyosis prematurity syndrome Is a Autosomal recessive hereditary disorder false Inferred relationship Some
Ichthyosis prematurity syndrome Associated morphology dysgenese false Inferred relationship Some 1
Ichthyosis prematurity syndrome Occurrence Congenital true Inferred relationship Some 1
Ichthyosis prematurity syndrome Finding site Skin structure false Inferred relationship Some 1
Ichthyosis prematurity syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Ichthyosis prematurity syndrome Associated morphology Hyperkeratosis true Inferred relationship Some 1
Ichthyosis prematurity syndrome Is a Autosomal recessive ichthyosis (disorder) true Inferred relationship Some
Ichthyosis prematurity syndrome Has interpretation Abnormal true Inferred relationship Some 2
Ichthyosis prematurity syndrome Interprets Keratinization true Inferred relationship Some 2
Ichthyosis prematurity syndrome Finding site Entire skin true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start