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

42530008: Xeroderma pigmentosum, group F (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1229883012 Xeroderma pigmentosum group F en Synonym Active Initial character case insensitive SNOMED CT core
70951017 Xeroderma pigmentosum, group F en Synonym Active Initial character case insensitive SNOMED CT core
779439010 Xeroderma pigmentosum, group F (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Xeroderma pigmentosum, group F Pathological process Pathological developmental process true Inferred relationship Some 3
Xeroderma pigmentosum, group F Interprets Moistness of skin true Inferred relationship Some 1
Xeroderma pigmentosum, group F Has interpretation Decreased true Inferred relationship Some 1
Xeroderma pigmentosum, group F Associated morphology Congenital anomaly false Inferred relationship Some 1
Xeroderma pigmentosum, group F Is a Xeroderma pigmentosum true Inferred relationship Some
Xeroderma pigmentosum, group F Finding site Skin structure false Inferred relationship Some 2
Xeroderma pigmentosum, group F Finding site Skin structure false Inferred relationship Some 2
Xeroderma pigmentosum, group F Finding site Skin structure false Inferred relationship Some 1
Xeroderma pigmentosum, group F Has definitional manifestation Abnormal keratinisation false Inferred relationship Some
Xeroderma pigmentosum, group F Associated morphology Papulovesicular eruption false Inferred relationship Some 3
Xeroderma pigmentosum, group F Finding site Skin structure false Inferred relationship Some 1
Xeroderma pigmentosum, group F Finding site Skin structure false Inferred relationship Some 1
Xeroderma pigmentosum, group F Finding site Skin structure false Inferred relationship Some 2
Xeroderma pigmentosum, group F Finding site Skin structure false Inferred relationship Some 4
Xeroderma pigmentosum, group F Finding site Skin structure true Inferred relationship Some 3
Xeroderma pigmentosum, group F Finding site Structure of skin region false Inferred relationship Some
Xeroderma pigmentosum, group F Associated morphology Pigment deposition false Inferred relationship Some 1
Xeroderma pigmentosum, group F Finding site Skin structure false Inferred relationship Some 1
Xeroderma pigmentosum, group F Associated morphology Congenital anomaly false Inferred relationship Some 1
Xeroderma pigmentosum, group F Finding site Skin structure false Inferred relationship Some 2
Xeroderma pigmentosum, group F Associated morphology Developmental abnormality false Inferred relationship Some 2
Xeroderma pigmentosum, group F Associated morphology Pigment deposition true Inferred relationship Some 3
Xeroderma pigmentosum, group F Associated morphology Pigment deposition false Inferred relationship Some 1
Xeroderma pigmentosum, group F Associated morphology Atrophy false Inferred relationship Some 4
Xeroderma pigmentosum, group F Finding site Skin structure false Inferred relationship Some 2
Xeroderma pigmentosum, group F Occurrence Congenital false Inferred relationship Some
Xeroderma pigmentosum, group F Associated morphology Degeneration false Inferred relationship Some 2
Xeroderma pigmentosum, group F Has interpretation Abnormal false Inferred relationship Some 1
Xeroderma pigmentosum, group F Interprets Keratinisation false Inferred relationship Some 1
Xeroderma pigmentosum, group F Interprets Moistness of skin false Inferred relationship Some 4

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