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399960008: Congenital hamartoma (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1767880010 Congenital hamartoma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1779241016 Congenital hamartoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3005817015 Congenital hamartosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3005821010 Hamartomatous disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3005858010 Hamartomatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1767880010 Congenital hamartoma (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1767880010 Congenital hamartoma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1779241016 Congenital hamartoma en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1779241016 Congenital hamartoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3005817015 Congenital hamartosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3005817015 Congenital hamartosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3005821010 Hamartomatous disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3005821010 Hamartomatous disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3005858010 Hamartomatosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3005858010 Hamartomatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
85081000077117 hamartome congénital fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
85081000077117 hamartome congénital fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

35 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital hamartoma (disorder) Is a Hamartoma (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hamartoma (disorder) Is a Congenital disease true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hamartoma (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hamartoma (disorder) Associated morphology Hamartoma false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hamartoma (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hamartoma (disorder) Associated morphology Hamartoma true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hamartoma (disorder) Is a Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hamartoma (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital diffuse lipomatosis (disorder) Is a False Congenital hamartoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Nevus comedonicus Is a False Congenital hamartoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome Is a True Congenital hamartoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Strawberry nevus of skin Is a False Congenital hamartoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hamartomatous disease Is a False Congenital hamartoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital pigmented melanocytic naevus Is a False Congenital hamartoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Deep hemangioma of skin Is a False Congenital hamartoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hamartoma of skin (disorder) Is a True Congenital hamartoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Gardner syndrome Is a True Congenital hamartoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Centrofacial lentiginosis syndrome Is a False Congenital hamartoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Neurocutaneous melanosis sequence Is a False Congenital hamartoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Ruvalcaba-Myhre syndrome Is a False Congenital hamartoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Turcot syndrome Is a False Congenital hamartoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Cowden syndrome Is a False Congenital hamartoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Is a False Congenital hamartoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Maffucci syndrome Is a False Congenital hamartoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Lhermitte-Duclos disease Is a True Congenital hamartoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
syndrome de Moynahan Is a False Congenital hamartoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Osler haemorrhagic telangiectasia syndrome Is a False Congenital hamartoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Goltz syndrome Is a False Congenital hamartoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Riley-Smith syndrome Is a False Congenital hamartoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Proteus syndrome Is a False Congenital hamartoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital erector pili hamartoma Is a False Congenital hamartoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Proteus like syndrome (disorder) Is a False Congenital hamartoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Perlman syndrome (disorder) Is a True Congenital hamartoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital rhabdomyomatous mesenchymal hamartoma Is a True Congenital hamartoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Tuberous sclerosis syndrome Is a False Congenital hamartoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Bilateral congenital hamartoma of irises Is a False Congenital hamartoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Fibrous skin tumor of tuberous sclerosis Is a True Congenital hamartoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Pulmonary tuberous sclerosis (disorder) Is a True Congenital hamartoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hamartoma of iris (disorder) Is a True Congenital hamartoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Cystic hamartoma of lung and kidney Is a True Congenital hamartoma (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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