FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

719819004: Xeroderma pigmentosum and Cockayne syndrome complex (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3318026011 Xeroderma pigmentosum and Cockayne syndrome complex (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3318028012 Xeroderma pigmentosum and Cockayne syndrome complex 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
Xeroderma pigmentosum and Cockayne syndrome complex Is a Cockayne syndrome true Inferred relationship Existential restriction modifier
Xeroderma pigmentosum and Cockayne syndrome complex Is a Xeroderma pigmentosum true Inferred relationship Existential restriction modifier
Xeroderma pigmentosum and Cockayne syndrome complex Is a Neuropathy false Inferred relationship Existential restriction modifier
Xeroderma pigmentosum and Cockayne syndrome complex Has definitional manifestation Abnormal keratinization false Inferred relationship Existential restriction modifier
Xeroderma pigmentosum and Cockayne syndrome complex Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 6
Xeroderma pigmentosum and Cockayne syndrome complex Finding site Skin structure false Inferred relationship Existential restriction modifier 6
Xeroderma pigmentosum and Cockayne syndrome complex Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 4
Xeroderma pigmentosum and Cockayne syndrome complex Occurrence Congenital false Inferred relationship Existential restriction modifier 4
Xeroderma pigmentosum and Cockayne syndrome complex Finding site Central nervous system tract structure false Inferred relationship Existential restriction modifier 4
Xeroderma pigmentosum and Cockayne syndrome complex Finding site Skin structure false Inferred relationship Existential restriction modifier 5
Xeroderma pigmentosum and Cockayne syndrome complex Associated morphology Structure showing abnormal deposition of pigment false Inferred relationship Existential restriction modifier 5
Xeroderma pigmentosum and Cockayne syndrome complex Has interpretation Abnormal false Inferred relationship Existential restriction modifier 3
Xeroderma pigmentosum and Cockayne syndrome complex Interprets Keratinization, function false Inferred relationship Existential restriction modifier 3
Xeroderma pigmentosum and Cockayne syndrome complex Interprets Moistness of skin false Inferred relationship Existential restriction modifier 4
Xeroderma pigmentosum and Cockayne syndrome complex Associated morphology Structure showing abnormal deposition of pigment true Inferred relationship Existential restriction modifier 2
Xeroderma pigmentosum and Cockayne syndrome complex Finding site Skin structure true Inferred relationship Existential restriction modifier 2
Xeroderma pigmentosum and Cockayne syndrome complex Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Xeroderma pigmentosum and Cockayne syndrome complex Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Xeroderma pigmentosum and Cockayne syndrome complex Finding site Central nervous system tract structure true Inferred relationship Existential restriction modifier 1
Xeroderma pigmentosum and Cockayne syndrome complex Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Xeroderma pigmentosum and Cockayne syndrome complex Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Xeroderma pigmentosum and Cockayne syndrome complex Interprets Moistness of skin true Inferred relationship Existential restriction modifier 3
Xeroderma pigmentosum and Cockayne syndrome complex Has interpretation Decreased 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