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718122005: Piebaldism (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3311230010 Piebaldism (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3311231014 Piebaldism 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
Piebaldism Is a Congenital deficiency of pigment of skin true Inferred relationship Existential restriction modifier
Piebaldism Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Piebaldism Is a Hereditary disorder of the integument true Inferred relationship Existential restriction modifier
Piebaldism Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 1
Piebaldism Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Piebaldism Finding site Skin structure true Inferred relationship Existential restriction modifier 1
Piebaldism Is a Genetic disorder of skin pigmentation true Inferred relationship Existential restriction modifier
Piebaldism Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Piebaldism Associated morphology Hypopigmentation true Inferred relationship Existential restriction modifier 1
Piebaldism Is a Developmental hereditary disorder 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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