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88877002: Xeroderma pigmentosum, variant form (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
1235388013 Xeroderma pigmentosum XP variant en Synonym Active Initial character case insensitive SNOMED CT core
147363011 Xeroderma pigmentosum, variant form en Synonym Active Case insensitive SNOMED CT core
5145538017 Pigmented xerodermoid en Synonym Active Case insensitive SNOMED CT core
831652015 Xeroderma pigmentosum, variant form (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


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

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