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774066000: Familial angiolipomatosis (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3727850017 Familial angiolipomatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3727851018 Familial angiolipomatosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3727852013 A rare genetic subcutaneous tissue disorder with the presence of benign usually multiple subcutaneous tumors. The tumors are composed of adipose tissue and blood vessels typically manifesting as yellow firm circumscribed 1-4 cm in diameter tumors located in the arms, legs and trunk with deep extension of the lesions between muscles, tendons and joint capsules (without infiltration of these structures) in several members of a single family. Tumors may be tender or mildly painful when palpated and do not regress spontaneously. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3727853015 A rare genetic subcutaneous tissue disorder with the presence of benign usually multiple subcutaneous tumours. The tumours are composed of adipose tissue and blood vessels typically manifesting as yellow firm circumscribed 1-4 cm in diameter tumours located in the arms, legs and trunk with deep extension of the lesions between muscles, tendons and joint capsules (without infiltration of these structures) in several members of a single family. Tumours may be tender or mildly painful when palpated and do not regress spontaneously. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3727850017 Familial angiolipomatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3727851018 Familial angiolipomatosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3727852013 A rare genetic subcutaneous tissue disorder with the presence of benign usually multiple subcutaneous tumors. The tumors are composed of adipose tissue and blood vessels typically manifesting as yellow firm circumscribed 1-4 cm in diameter tumors located in the arms, legs and trunk with deep extension of the lesions between muscles, tendons and joint capsules (without infiltration of these structures) in several members of a single family. Tumors may be tender or mildly painful when palpated and do not regress spontaneously. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3727853015 A rare genetic subcutaneous tissue disorder with the presence of benign usually multiple subcutaneous tumours. The tumours are composed of adipose tissue and blood vessels typically manifesting as yellow firm circumscribed 1-4 cm in diameter tumours located in the arms, legs and trunk with deep extension of the lesions between muscles, tendons and joint capsules (without infiltration of these structures) in several members of a single family. Tumours may be tender or mildly painful when palpated and do not regress spontaneously. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3423271001000111 Angiolipomatose, familiäre de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
936311000172112 angiolipomatose familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
936311000172112 angiolipomatose familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3423271001000111 Angiolipomatose, familiäre de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial angiolipomatosis Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Familial angiolipomatosis Finding site Subcutaneous tissue structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial angiolipomatosis Is a Angiolipoma (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Familial angiolipomatosis Associated morphology Angiolipoma true Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial angiolipomatosis Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Familial angiolipomatosis Is a Hereditary disorder of the integument (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Familial angiolipomatosis Is a Familial neoplastic disease true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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