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238764001: Hereditary benign telangiectasia (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
357850018 Hereditary benign telangiectasia en Synonym Active Entire term case insensitive SNOMED CT core module
627688013 Hereditary benign telangiectasia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary benign telangiectasia Is a Primary idiopathic cutaneous telangiectasia false Inferred relationship Existential restriction modifier
Hereditary benign telangiectasia Finding site Blood vessel structure false Inferred relationship Existential restriction modifier
Hereditary benign telangiectasia Finding site Skin structure false Inferred relationship Existential restriction modifier
Hereditary benign telangiectasia Finding site Peripheral vascular system structure false Inferred relationship Existential restriction modifier
Hereditary benign telangiectasia Associated morphology Telangiectasis false Inferred relationship Existential restriction modifier 1
Hereditary benign telangiectasia Finding site Microscopic skin vascular structure false Inferred relationship Existential restriction modifier 1
Hereditary benign telangiectasia Finding site Microscopic skin vascular structure false Inferred relationship Existential restriction modifier 1
Hereditary benign telangiectasia Associated morphology Telangiectasis true Inferred relationship Existential restriction modifier 1
Hereditary benign telangiectasia Is a Cardiovascular system hereditary disorder true Inferred relationship Existential restriction modifier
Hereditary benign telangiectasia Is a Telangiectasia disorder true Inferred relationship Existential restriction modifier
Hereditary benign telangiectasia Is a Hereditary disorder of the integument false Inferred relationship Existential restriction modifier
Hereditary benign telangiectasia Finding site Blood vessel structure 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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