FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.24  |  FHIR Version n/a  User: [n/a]

763368004: Familial progressive hyperpigmentation and hypopigmentation of skin (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3640240015 Familial progressive hyperpigmentation and hypopigmentation of skin en Synonym Active Entire term case insensitive SNOMED CT core module
3640241016 Familial progressive hyper and hypopigmentation en Synonym Active Entire term case insensitive SNOMED CT core module
3640242011 Familial progressive hyperpigmentation and hypopigmentation of skin (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
Familial progressive hyperpigmentation and hypopigmentation of skin Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Familial progressive hyperpigmentation and hypopigmentation of skin Is a Congenital pigmentary skin anomalies true Inferred relationship Existential restriction modifier
Familial progressive hyperpigmentation and hypopigmentation of skin Is a Genetic disorder of skin pigmentation true Inferred relationship Existential restriction modifier
Familial progressive hyperpigmentation and hypopigmentation of skin Associated morphology Pigment alteration false Inferred relationship Existential restriction modifier 2
Familial progressive hyperpigmentation and hypopigmentation of skin Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Familial progressive hyperpigmentation and hypopigmentation of skin Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Familial progressive hyperpigmentation and hypopigmentation of skin Finding site Skin structure true Inferred relationship Existential restriction modifier 1
Familial progressive hyperpigmentation and hypopigmentation of skin Associated morphology Pigment alteration true Inferred relationship Existential restriction modifier 1
Familial progressive hyperpigmentation and hypopigmentation of skin Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Familial progressive hyperpigmentation and hypopigmentation of skin Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
Familial progressive hyperpigmentation and hypopigmentation of skin Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Familial progressive hyperpigmentation and hypopigmentation of skin Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Familial progressive hyperpigmentation and hypopigmentation of skin Is a Hereditary disorder of the integument true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start