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766812005: Trichodysplasia xeroderma syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3662697014 Trichodysplasia xeroderma syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3662698016 Trichodysplasia xeroderma syndrome en Synonym Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Trichodysplasia xeroderma syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Trichodysplasia xeroderma syndrome Is a Xeroderma true Inferred relationship Existential restriction modifier
Trichodysplasia xeroderma syndrome Interprets Keratinization, function false Inferred relationship Existential restriction modifier 3
Trichodysplasia xeroderma syndrome Finding site Hair shaft structure false Inferred relationship Existential restriction modifier 1
Trichodysplasia xeroderma syndrome Interprets Moistness of skin true Inferred relationship Existential restriction modifier 1
Trichodysplasia xeroderma syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Trichodysplasia xeroderma syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 1
Trichodysplasia xeroderma syndrome Has interpretation Abnormal false Inferred relationship Existential restriction modifier 3
Trichodysplasia xeroderma syndrome Is a Genetic defect of hair shaft true Inferred relationship Existential restriction modifier
Trichodysplasia xeroderma syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
Trichodysplasia xeroderma syndrome Is a Hereditary disorder of the integument true Inferred relationship Existential restriction modifier
Trichodysplasia xeroderma syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Trichodysplasia xeroderma syndrome Finding site Hair shaft structure true Inferred relationship Existential restriction modifier 2
Trichodysplasia xeroderma syndrome Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 1
Trichodysplasia xeroderma syndrome Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier 1
Trichodysplasia xeroderma syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Trichodysplasia xeroderma syndrome Is a Inherited disorder of keratinization false Inferred relationship Existential restriction modifier
Trichodysplasia xeroderma syndrome Is a Keratosis false Inferred relationship Existential restriction modifier
Trichodysplasia xeroderma syndrome Associated morphology Defect true Inferred relationship Existential restriction modifier 2
Trichodysplasia xeroderma syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Trichodysplasia xeroderma syndrome Has interpretation Decreased true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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