FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

783013001: Parana hard skin syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3757143017 Parana hard skin syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3757144011 Parana hard skin syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3757145012 Hard skin syndrome Parana type en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Parana hard skin syndrome Is a Thickening of skin true Inferred relationship Existential restriction modifier
Parana hard skin syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Parana hard skin syndrome Is a Chronic disease of skin true Inferred relationship Existential restriction modifier
Parana hard skin syndrome Is a Hereditary disorder of the integument true Inferred relationship Existential restriction modifier
Parana hard skin syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Parana hard skin syndrome Is a Chronic arthropathy true Inferred relationship Existential restriction modifier
Parana hard skin syndrome Finding site Joint structure true Inferred relationship Existential restriction modifier 2
Parana hard skin syndrome Clinical course Progressive true Inferred relationship Existential restriction modifier 1
Parana hard skin syndrome Finding site Skin structure true Inferred relationship Existential restriction modifier 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start