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88877002: Xeroderma pigmentosum, variant form (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module Reference Sets
147363011 Xeroderma pigmentosum, variant form en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
831652015 Xeroderma pigmentosum, variant form (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
1235388013 Xeroderma pigmentosum XP variant en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)

0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Xeroderma pigmentosum, variant form Is a Xeroderma pigmentosum true Inferred relationship Some
Xeroderma pigmentosum, variant form Occurrence Congenital false Inferred relationship Some
Xeroderma pigmentosum, variant form Has definitional manifestation Abnormal keratinization false Inferred relationship Some
Xeroderma pigmentosum, variant form Finding site Structure of skin region false Inferred relationship Some
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 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 Papulovesicular rash 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 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 1
Xeroderma pigmentosum, variant form Associated morphology Pigment deposition false Inferred relationship Some 1
Xeroderma pigmentosum, variant form Has interpretation Abnormal true Inferred relationship Some 1
Xeroderma pigmentosum, variant form Interprets Keratinization true Inferred relationship Some 1
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 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 true Inferred relationship Some 2
Xeroderma pigmentosum, variant form Associated morphology Developmental anomaly (morphologic abnormality) true Inferred relationship Some 2
Xeroderma pigmentosum, variant form Finding site Skin structure true Inferred relationship Some 3
Xeroderma pigmentosum, variant form Associated morphology Pigment deposition true Inferred relationship Some 3
Xeroderma pigmentosum, variant form Associated morphology Atrophy false Inferred relationship Some 4
Xeroderma pigmentosum, variant form Finding site Skin structure false Inferred relationship Some 4
Xeroderma pigmentosum, variant form Interprets Moistness of skin true Inferred relationship Some 4

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Description inactivation indicator reference set

GB English

US English

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