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733491005: Carney complex (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3499549016 Carney complex (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3499550016 Carney complex en Synonym Active Entire term case sensitive SNOMED CT core module
3499551017 Carney syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3499552012 Myxoma, spotty pigmentation, endocrine overactivity syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
5074414016 LAMB (lentigines, atrial myxoma, blue nevi) syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
5084982014 LAMB (lentigines, atrial myxoma, blue naevi) 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
Carney complex Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Carney complex Is a Congenital pigmentary skin anomalies true Inferred relationship Existential restriction modifier
Carney complex Is a Polyglandular hyperfunction true Inferred relationship Existential restriction modifier
Carney complex Is a Degenerative disorder false Inferred relationship Existential restriction modifier
Carney complex Is a Cardiovascular system hereditary disorder true Inferred relationship Existential restriction modifier
Carney complex Is a Hereditary disorder of endocrine system true Inferred relationship Existential restriction modifier
Carney complex Is a Myxoma of heart true Inferred relationship Existential restriction modifier
Carney complex Is a Genetic disorder of skin pigmentation true Inferred relationship Existential restriction modifier
Carney complex Associated morphology Myxomatous neoplasm false Inferred relationship Existential restriction modifier 3
Carney complex Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Carney complex Finding site Heart structure false Inferred relationship Existential restriction modifier 3
Carney complex Occurrence Congenital false Inferred relationship Existential restriction modifier 4
Carney complex Finding site Structure of multiple endocrine glands false Inferred relationship Existential restriction modifier 4
Carney complex Associated morphology Congenital hyperpigmentation false Inferred relationship Existential restriction modifier 5
Carney complex Occurrence Congenital false Inferred relationship Existential restriction modifier 5
Carney complex Finding site Skin structure false Inferred relationship Existential restriction modifier 5
Carney complex Finding site Structure of multiple endocrine glands true Inferred relationship Existential restriction modifier 3
Carney complex Is a Congenital cardiovascular disorder true Inferred relationship Existential restriction modifier
Carney complex Is a Congenital heart disease false Inferred relationship Existential restriction modifier
Carney complex Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Carney complex Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Carney complex Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 1
Carney complex Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Carney complex Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Carney complex Associated morphology Myxomatous neoplasm true Inferred relationship Existential restriction modifier 1
Carney complex Finding site Skin structure true Inferred relationship Existential restriction modifier 2
Carney complex Finding site Heart structure true Inferred relationship Existential restriction modifier 1
Carney complex Associated morphology Hyperpigmentation true Inferred relationship Existential restriction modifier 2
Carney complex Is a Hyperpigmentation of skin true Inferred relationship Existential restriction modifier
Carney complex Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Carney complex 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

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