774066000: Familial angiolipomatosis (disorder)

SNOMED CT Concept\Clinical finding\...

\Mass of body structure\Mass of soft tissue\Mass of subcutaneous tissue\Subcutaneous lipoma\Angiolipoma\Familial angiolipomatosis
\Mass of body structure\Mass of soft tissue\Neoplasm of soft tissue\Benign neoplasm of soft tissue\Lipoma of skin and subcutaneous tissue\Subcutaneous lipoma\Angiolipoma\Familial angiolipomatosis
\Mass of body structure\Neoplasm of integumentary system\Lipoma of skin and subcutaneous tissue\Subcutaneous lipoma\Angiolipoma\Familial angiolipomatosis
\Mass of body structure\Mass of body region\Mass of subcutaneous tissue\Subcutaneous lipoma\Angiolipoma\Familial angiolipomatosis
\Mass of body structure\Mass of body region\Lipoma of skin and subcutaneous tissue\Subcutaneous lipoma\Angiolipoma\Familial angiolipomatosis

\General finding of soft tissue\Mass of soft tissue\Mass of subcutaneous tissue\Subcutaneous lipoma\Angiolipoma\Familial angiolipomatosis
\General finding of soft tissue\Mass of soft tissue\Neoplasm of soft tissue\Benign neoplasm of soft tissue\Lipoma of skin and subcutaneous tissue\Subcutaneous lipoma\Angiolipoma\Familial angiolipomatosis
\General finding of soft tissue\Subcutaneous tissue finding\Mass of subcutaneous tissue\Subcutaneous lipoma\Angiolipoma\Familial angiolipomatosis
\General finding of soft tissue\Subcutaneous tissue finding\Disorder of subcutaneous tissue\Subcutaneous lipoma\Angiolipoma\Familial angiolipomatosis
\General finding of soft tissue\Disorder of soft tissue\Soft tissue lesion\Neoplasm of soft tissue\Benign neoplasm of soft tissue\Lipoma of skin and subcutaneous tissue\Subcutaneous lipoma\Angiolipoma\Familial angiolipomatosis
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Lipoma of skin and subcutaneous tissue\Subcutaneous lipoma\Angiolipoma\Familial angiolipomatosis
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of subcutaneous tissue\Subcutaneous lipoma\Angiolipoma\Familial angiolipomatosis

\Integumentary system finding\Subcutaneous tissue finding\Mass of subcutaneous tissue\Subcutaneous lipoma\Angiolipoma\Familial angiolipomatosis
\Integumentary system finding\Subcutaneous tissue finding\Disorder of subcutaneous tissue\Subcutaneous lipoma\Angiolipoma\Familial angiolipomatosis
\Integumentary system finding\Disorder of integument\Neoplasm of integumentary system\Lipoma of skin and subcutaneous tissue\Subcutaneous lipoma\Angiolipoma\Familial angiolipomatosis
\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Familial angiolipomatosis
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Lipoma of skin and subcutaneous tissue\Subcutaneous lipoma\Angiolipoma\Familial angiolipomatosis
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of subcutaneous tissue\Subcutaneous lipoma\Angiolipoma\Familial angiolipomatosis

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Familial angiolipomatosis
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Familial angiolipomatosis
\Disease\Neoplasm and/or hamartoma\Neoplastic disease\Neoplasm of integumentary system\Lipoma of skin and subcutaneous tissue\Subcutaneous lipoma\Angiolipoma\Familial angiolipomatosis
\Disease\Neoplasm and/or hamartoma\Neoplastic disease\Neoplasm of soft tissue\Benign neoplasm of soft tissue\Lipoma of skin and subcutaneous tissue\Subcutaneous lipoma\Angiolipoma\Familial angiolipomatosis
\Disease\Neoplasm and/or hamartoma\Neoplastic disease\Lipomatous tumour\Benign lipomatous tumour\Lipoma\Lipoma of skin and subcutaneous tissue\Subcutaneous lipoma\Angiolipoma\Familial angiolipomatosis
\Disease\Neoplasm and/or hamartoma\Neoplastic disease\Familial neoplastic disease\Familial angiolipomatosis
\Disease\Neoplasm and/or hamartoma\Neoplastic disease\Benign neoplastic disease\Benign lipomatous tumour\Lipoma\Lipoma of skin and subcutaneous tissue\Subcutaneous lipoma\Angiolipoma\Familial angiolipomatosis
\Disease\Neoplasm and/or hamartoma\Neoplastic disease\Benign neoplastic disease\Benign neoplasm of soft tissue\Lipoma of skin and subcutaneous tissue\Subcutaneous lipoma\Angiolipoma\Familial angiolipomatosis
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Familial angiolipomatosis
\Disease\Disorder of body system\Disorder of integument\Neoplasm of integumentary system\Lipoma of skin and subcutaneous tissue\Subcutaneous lipoma\Angiolipoma\Familial angiolipomatosis
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Familial angiolipomatosis
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Lipoma of skin and subcutaneous tissue\Subcutaneous lipoma\Angiolipoma\Familial angiolipomatosis
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of subcutaneous tissue\Subcutaneous lipoma\Angiolipoma\Familial angiolipomatosis
\Disease\Familial disease\Familial neoplastic disease\Familial angiolipomatosis
\Disease\Disorder of soft tissue\Soft tissue lesion\Neoplasm of soft tissue\Benign neoplasm of soft tissue\Lipoma of skin and subcutaneous tissue\Subcutaneous lipoma\Angiolipoma\Familial angiolipomatosis
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Lipoma of skin and subcutaneous tissue\Subcutaneous lipoma\Angiolipoma\Familial angiolipomatosis
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of subcutaneous tissue\Subcutaneous lipoma\Angiolipoma\Familial angiolipomatosis

Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3727850017 Familial angiolipomatosis en Synonym Active Case insensitive SNOMED CT core

3727851018 Familial angiolipomatosis (disorder) en Fully specified name Active Case insensitive 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 Case sensitive 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 Case sensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial angiolipomatosis	Is a	Inherited disorder of connective tissue	false	Inferred relationship	Some
Familial angiolipomatosis	Finding site	Subcutaneous tissue structure	true	Inferred relationship	Some	1
Familial angiolipomatosis	Is a	Angiolipoma	true	Inferred relationship	Some
Familial angiolipomatosis	Associated morphology	Angiolipoma	true	Inferred relationship	Some	1
Familial angiolipomatosis	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Familial angiolipomatosis	Is a	Hereditary disorder of the integument	true	Inferred relationship	Some
Familial angiolipomatosis	Is a	Familial neoplastic disease	true	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Neoplasm and/or hamartoma reference set

Problem/Diagnosis reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3727850017	Familial angiolipomatosis	en	Synonym	Active	Case insensitive	SNOMED CT core
3727851018	Familial angiolipomatosis (disorder)	en	Fully specified name	Active	Case insensitive	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	Case sensitive	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	Case sensitive	SNOMED CT core