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69408002: Gorlin syndrome (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2003. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
115299010 Gorlin syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
115300019 Nevoid basal cell carcinoma syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
115301015 Basal cell carcinoma syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
115302010 Gorlin-Goltz syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
115303017 Basal cell nevus syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
501272016 Naevoid basal cell carcinoma syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
501273014 Basal cell naevus syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
809350016 Gorlin syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
1216871010 BCNS - Basal cell naevus syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
1216872015 NBCCS - Naevoid basal cell carcinoma syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
1218358013 NBCCS - Nevoid basal cell carcinoma syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
1218359017 BCNS - Basal cell nevus syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
1233157019 Gorlin's syndrome en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Gorlin syndrome Is a Hereditary disorder of the integument true Inferred relationship Existential restriction modifier
Gorlin syndrome Is a Basal cell carcinoma of skin true Inferred relationship Existential restriction modifier
Gorlin syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Gorlin syndrome Pathological process Neoplastic process false Inferred relationship Existential restriction modifier
Gorlin syndrome Pathological process Malignant neoplastic process false Inferred relationship Existential restriction modifier
Gorlin syndrome Associated morphology Basal cell carcinoma false Inferred relationship Existential restriction modifier 1
Gorlin syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Gorlin syndrome Finding site Structure of skin region false Inferred relationship Existential restriction modifier 2
Gorlin syndrome Associated morphology Malignant neoplasm, primary false Inferred relationship Existential restriction modifier 2
Gorlin syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Gorlin syndrome Is a Familial multiple tumor syndrome false Inferred relationship Existential restriction modifier
Gorlin syndrome Is a Primary malignant neoplasm false Inferred relationship Existential restriction modifier
Gorlin syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Gorlin syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Gorlin syndrome Associated morphology Basal cell carcinoma in basal cell nevus syndrome false Inferred relationship Existential restriction modifier 1
Gorlin syndrome Is a Primary malignant neoplasm of soft tissues false Inferred relationship Existential restriction modifier
Gorlin syndrome Is a Primary malignant neoplasm of skin false Inferred relationship Existential restriction modifier
Gorlin syndrome Associated morphology Basal cell carcinoma in basal cell nevus syndrome true Inferred relationship Existential restriction modifier 1
Gorlin syndrome Finding site Skin structure true Inferred relationship Existential restriction modifier 1
Gorlin syndrome Is a Hereditary cancer-predisposing syndrome true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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