FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.2  |  FHIR Version n/a  User: [n/a]

723001002: Hypohidrosis due to genetic abnormality of eccrine gland structure and function (disorder)


Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3334123019 Hypohidrosis due to genetic abnormality of eccrine gland structure and function (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3334124013 Hypohidrosis due to genetic abnormality of eccrine gland structure and function en Synonym Active Case insensitive SNOMED CT core
3334125014 Hereditary hypohidrosis en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hypohidrosis due to genetic abnormality of eccrine gland structure and function Has interpretation Decreased true Inferred relationship Some 2
Hypohidrosis due to genetic abnormality of eccrine gland structure and function Interprets Sweating true Inferred relationship Some 2
Hypohidrosis due to genetic abnormality of eccrine gland structure and function Is a Hypohidrosis true Inferred relationship Some
Hypohidrosis due to genetic abnormality of eccrine gland structure and function Is a Hereditary disorder of the integument true Inferred relationship Some
Hypohidrosis due to genetic abnormality of eccrine gland structure and function Finding site Sweat gland structure true Inferred relationship Some 1
Hypohidrosis due to genetic abnormality of eccrine gland structure and function Finding site Skin structure false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start