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58037000: Cowden syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
96476011 Cowden syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
96477019 Multiple hamartoma syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
796725015 Cowden syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
1231795010 Cowden'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
Cowden syndrome Is a Congenital anomaly of trunk false Inferred relationship Existential restriction modifier
Cowden syndrome Is a Congenital anomaly of digestive system false Inferred relationship Existential restriction modifier
Cowden syndrome Is a Congenital hamartosis false Inferred relationship Existential restriction modifier
Cowden syndrome Is a Intestinal polyposis syndrome true Inferred relationship Existential restriction modifier
Cowden syndrome Is a Multisystem disorder M-N false Inferred relationship Existential restriction modifier
Cowden syndrome Is a Familial multiple tumor syndrome false Inferred relationship Existential restriction modifier
Cowden syndrome Associated morphology Hamartoma false Inferred relationship Existential restriction modifier
Cowden syndrome Finding site Intestinal structure false Inferred relationship Existential restriction modifier 1
Cowden syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Cowden syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier
Cowden syndrome Is a Multisystem disorder false Inferred relationship Existential restriction modifier
Cowden syndrome Associated morphology Neoplasm false Inferred relationship Existential restriction modifier
Cowden syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Cowden syndrome Associated morphology Polyp false Inferred relationship Existential restriction modifier 1
Cowden syndrome Finding site Intestinal structure true Inferred relationship Existential restriction modifier 1
Cowden syndrome Associated morphology Polyp true Inferred relationship Existential restriction modifier 1
Cowden syndrome Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier
Cowden syndrome Is a Congenital hamartoma false Inferred relationship Existential restriction modifier
Cowden syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Cowden syndrome Associated morphology Hamartoma true Inferred relationship Existential restriction modifier 2
Cowden syndrome Is a PTEN hamartoma tumor syndrome true Inferred relationship Existential restriction modifier
Cowden syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Cowden syndrome Finding site Skin structure true Inferred relationship Existential restriction modifier 2
Cowden syndrome Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 2
Cowden syndrome Is a Congenital anomaly of intestinal tract true Inferred relationship Existential restriction modifier
Cowden syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Family history of Cowden syndrome Associated finding True Cowden syndrome Inferred relationship Existential restriction modifier 1
Gingival enlargement due to Cowden syndrome Due to True Cowden syndrome Inferred relationship Existential restriction modifier 2

This concept is not in any reference sets

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