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766881008: Carney complex, trismus, pseudocamptodactyly syndrome (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
3663000011 Carney complex, trismus, pseudocamptodactyly syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3663001010 Carney complex variant en Synonym Active Entire term case sensitive SNOMED CT core module
3663002015 Carney complex, trismus, pseudocamptodactyly syndrome (disorder) en Fully specified name 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, trismus, pseudocamptodactyly syndrome Is a Dysostosis true Inferred relationship Existential restriction modifier
Carney complex, trismus, pseudocamptodactyly syndrome Is a Congenital pigmentary skin anomalies true Inferred relationship Existential restriction modifier
Carney complex, trismus, pseudocamptodactyly syndrome Finding site Heart structure true Inferred relationship Existential restriction modifier 1
Carney complex, trismus, pseudocamptodactyly syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Carney complex, trismus, pseudocamptodactyly syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Carney complex, trismus, pseudocamptodactyly syndrome Associated morphology Congenital hyperpigmentation false Inferred relationship Existential restriction modifier 2
Carney complex, trismus, pseudocamptodactyly syndrome Is a Myxoma of heart true Inferred relationship Existential restriction modifier
Carney complex, trismus, pseudocamptodactyly syndrome Associated morphology Myxomatous neoplasm true Inferred relationship Existential restriction modifier 1
Carney complex, trismus, pseudocamptodactyly syndrome Is a Congenital anomaly of limb true Inferred relationship Existential restriction modifier
Carney complex, trismus, pseudocamptodactyly syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Carney complex, trismus, pseudocamptodactyly syndrome Is a Congenital cardiovascular disorder true Inferred relationship Existential restriction modifier
Carney complex, trismus, pseudocamptodactyly syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Carney complex, trismus, pseudocamptodactyly syndrome Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Existential restriction modifier
Carney complex, trismus, pseudocamptodactyly syndrome Is a Degenerative disorder false Inferred relationship Existential restriction modifier
Carney complex, trismus, pseudocamptodactyly syndrome Finding site Bone structure of extremity false Inferred relationship Existential restriction modifier 1
Carney complex, trismus, pseudocamptodactyly syndrome Finding site Skin structure true Inferred relationship Existential restriction modifier 3
Carney complex, trismus, pseudocamptodactyly syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
Carney complex, trismus, pseudocamptodactyly syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 2
Carney complex, trismus, pseudocamptodactyly syndrome Finding site Bone structure of extremity true Inferred relationship Existential restriction modifier 2
Carney complex, trismus, pseudocamptodactyly syndrome Associated morphology Myxomatous neoplasm false Inferred relationship Existential restriction modifier 3
Carney complex, trismus, pseudocamptodactyly syndrome Finding site Heart structure false Inferred relationship Existential restriction modifier 3
Carney complex, trismus, pseudocamptodactyly syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Carney complex, trismus, pseudocamptodactyly syndrome Is a Congenital heart disease false Inferred relationship Existential restriction modifier
Carney complex, trismus, pseudocamptodactyly syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Carney complex, trismus, pseudocamptodactyly syndrome Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 1
Carney complex, trismus, pseudocamptodactyly syndrome Associated morphology Hyperpigmentation true Inferred relationship Existential restriction modifier 3
Carney complex, trismus, pseudocamptodactyly syndrome Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 2
Carney complex, trismus, pseudocamptodactyly syndrome Is a Hyperpigmentation of skin 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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