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733491005: Carney complex (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
3499549016 Carney complex (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3499550016 Carney complex en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3499551017 Carney syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3499552012 Myxoma, spotty pigmentation, endocrine overactivity syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5074414016 LAMB (lentigines, atrial myxoma, blue nevi) syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5084982014 LAMB (lentigines, atrial myxoma, blue naevi) syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403807011 A rare endocrine disease characterized by lentigines with a specific peri-orifical distribution, blue nevus, myxomas, various endocrine tumors including primary pigmented nodular adrenocortical disease (PPNAD), acromegaly, thyroid tumors, and a wide range of other tumors. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403808018 A rare endocrine disease characterised by lentigines with a specific peri-orifical distribution, blue naevus, myxomas, various endocrine tumours including primary pigmented nodular adrenocortical disease (PPNAD), acromegaly, thyroid tumours, and a wide range of other tumours. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

1 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Carney complex (disorder) Is a Autosomal dominant hereditary disorder false Inferred relationship Some
Carney complex (disorder) Is a Congenital pigmentary skin anomalies false Inferred relationship Some
Carney complex (disorder) Is a Polyglandular hyperfunction true Inferred relationship Some
Carney complex (disorder) Is a Degenerative disorder false Inferred relationship Some
Carney complex (disorder) Is a Cardiovascular system hereditary disorder false Inferred relationship Some
Carney complex (disorder) Is a Hereditary disorder of endocrine system (disorder) false Inferred relationship Some
Carney complex (disorder) Is a Myxoma of heart (disorder) true Inferred relationship Some
Carney complex (disorder) Is a Genetic disorder of skin pigmentation (disorder) true Inferred relationship Some
Carney complex (disorder) Associated morphology Myxomatous neoplasm false Inferred relationship Some 3
Carney complex (disorder) Occurrence Congenital false Inferred relationship Some 3
Carney complex (disorder) Finding site Heart structure false Inferred relationship Some 3
Carney complex (disorder) Occurrence Congenital false Inferred relationship Some 4
Carney complex (disorder) Finding site Structure of multiple endocrine glands false Inferred relationship Some 4
Carney complex (disorder) Associated morphology Congenital hyperpigmentation false Inferred relationship Some 5
Carney complex (disorder) Occurrence Congenital false Inferred relationship Some 5
Carney complex (disorder) Finding site Skin structure false Inferred relationship Some 5
Carney complex (disorder) Finding site Structure of multiple endocrine glands true Inferred relationship Some 3
Carney complex (disorder) Is a Congenital cardiovascular disorder (disorder) false Inferred relationship Some
Carney complex (disorder) Is a Congenital heart disease false Inferred relationship Some
Carney complex (disorder) Pathological process (attribute) Pathological developmental process false Inferred relationship Some 3
Carney complex (disorder) Occurrence Congenital false Inferred relationship Some 1
Carney complex (disorder) Pathological process (attribute) Pathological developmental process false Inferred relationship Some 1
Carney complex (disorder) Pathological process (attribute) Pathological developmental process false Inferred relationship Some 2
Carney complex (disorder) Occurrence Congenital false Inferred relationship Some 2
Carney complex (disorder) Associated morphology Myxomatous neoplasm true Inferred relationship Some 1
Carney complex (disorder) Finding site Skin structure true Inferred relationship Some 2
Carney complex (disorder) Finding site Heart structure true Inferred relationship Some 1
Carney complex (disorder) Associated morphology Hyperpigmentation true Inferred relationship Some 2
Carney complex (disorder) Is a Hyperpigmentation of skin true Inferred relationship Some
Carney complex (disorder) Is a Developmental hereditary disorder false Inferred relationship Some
Carney complex (disorder) Is a Hereditary disorder of the integument false Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Carney complex-associated-primary pigmented nodular adrenocortical disease (disorder) Is a True Carney complex (disorder) Inferred relationship Some

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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