FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

718122005: Piebaldism (disorder)


Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3311230010 Piebaldism (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3311231014 Piebaldism en Synonym Active Case insensitive SNOMED CT core
3311232019 Piebaldism is a rare congenital pigmentation skin disorder with characteristic of the presence of hypopigmented and depigmented skin areas (leukoderma) on various parts of the body, preferentially on the forehead, chest, abdomen, upper arms, and lower extremities, that are associated with a white forelock (poliosis), and in some cases with hypopigmented and depigmented eyebrows and eyelashes. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Piebaldism Pathological process Pathological developmental process true Inferred relationship Some 1
Piebaldism Associated morphology Hypopigmentation true Inferred relationship Some 1
Piebaldism Is a Developmental hereditary disorder true Inferred relationship Some
Piebaldism Is a Congenital deficiency of pigment of skin true Inferred relationship Some
Piebaldism Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Piebaldism Is a Hereditary disorder of the integument true Inferred relationship Some
Piebaldism Associated morphology Congenital hypopigmentation false Inferred relationship Some 1
Piebaldism Occurrence Congenital true Inferred relationship Some 1
Piebaldism Finding site Skin structure true Inferred relationship Some 1
Piebaldism Is a Genetic disorder of skin pigmentation true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start