FHIR © HL7.org | Server Home | FHIR Server FHIR Server 3.8.3 | FHIR Version n/a User: [n/a]

360331008: Rhabdomyosarcoma - category (morphologic abnormality)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Oct 2021. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
rabdomyosarkom iht. kategori	Is a	Morphological descriptors	false	Inferred relationship	Some
rabdomyosarkom iht. kategori	Is a	rabdomyomatøst neoplasme iht. kategori	false	Inferred relationship	Some
rabdomyosarkom iht. kategori	Is a	Malignant myomatous tumour	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Rhabdomyosarcoma of orbit	Associated morphology	False	rabdomyosarkom iht. kategori	Inferred relationship	Some	1
Rhabdomyosarcoma of urinary bladder (disorder)	Associated morphology	False	rabdomyosarkom iht. kategori	Inferred relationship	Some	1
Spindle cell rhabdomyosarcoma	Is a	False	rabdomyosarkom iht. kategori	Inferred relationship	Some
Ectomesenchymoma (morphologic abnormality)	Is a	False	rabdomyosarkom iht. kategori	Inferred relationship	Some
Embryonal rhabdomyosarcoma	Is a	False	rabdomyosarkom iht. kategori	Inferred relationship	Some
Rhabdomyosarcoma	Is a	False	rabdomyosarkom iht. kategori	Inferred relationship	Some
Mixed type rhabdomyosarcoma	Is a	False	rabdomyosarkom iht. kategori	Inferred relationship	Some
Alveolar rhabdomyosarcoma	Is a	False	rabdomyosarkom iht. kategori	Inferred relationship	Some
Pleomorphic rhabdomyosarcoma	Is a	False	rabdomyosarkom iht. kategori	Inferred relationship	Some
[M]Rhabdomyosarcoma NOS	Is a	False	rabdomyosarkom iht. kategori	Inferred relationship	Some
Rhabdomyosarcoma of orbit	Associated morphology	False	rabdomyosarkom iht. kategori	Inferred relationship	Some	1
Rhabdomyosarcoma of urinary bladder (disorder)	Associated morphology	False	rabdomyosarkom iht. kategori	Inferred relationship	Some	1
Rhabdomyosarcoma (disorder)	Associated morphology	False	rabdomyosarkom iht. kategori	Inferred relationship	Some	1
Botryoid rhabdomyosarcoma (disorder)	Associated morphology	False	rabdomyosarkom iht. kategori	Inferred relationship	Some	1
rabdomyosarkom i bindevæv eller bløddel	Associated morphology	False	rabdomyosarkom iht. kategori	Inferred relationship	Some	1
Rhabdomyosarcoma of urinary bladder (disorder)	Associated morphology	False	rabdomyosarkom iht. kategori	Inferred relationship	Some	1
Rhabdomyosarcoma of the cervix uteri is a rare, highly malignant soft tissue sarcoma located in the uterine cervix and arising from primitive mesenchymal cells displaying skeletal muscle differentiation. It most often presents with abnormal vaginal discharge or dysfunctional uterine bleeding, abdominal pain and/or a cervical mass protruding into the vagina. Association with DICER1 syndrome has been reported.	Associated morphology	False	rabdomyosarkom iht. kategori	Inferred relationship	Some	1
Rhabdomyosarcoma of the corpus uteri is an extremely rare, highly malignant soft tissue sarcoma located in the uterine body and arising from primitive mesenchymal cells displaying variable degrees of skeletal muscle differentiation. It most often presents with abnormal vaginal discharge or dysfunctional uterine bleeding, abdominal pain and lower abdominal mass. Association with DICER1 syndrome has been reported.	Associated morphology	False	rabdomyosarkom iht. kategori	Inferred relationship	Some	1
Vulvovaginal rhabdomyosarcoma is a rare vulvovaginal tumor, a highly malignant soft tissue sarcoma composed of cells with round to oval or spindle-shaped nuclei and eosinophilic cytoplasm that may show differentiation towards striated muscle cells. It usually affects children and presents with a vulvar or vaginal mass that may be polypoid or grape-like (embryonal subtype) and associated with bleeding and ulceration.	Associated morphology	False	rabdomyosarkom iht. kategori	Inferred relationship	Some	1
Vulvovaginal rhabdomyosarcoma is a rare vulvovaginal tumor, a highly malignant soft tissue sarcoma composed of cells with round to oval or spindle-shaped nuclei and eosinophilic cytoplasm that may show differentiation towards striated muscle cells. It usually affects children and presents with a vulvar or vaginal mass that may be polypoid or grape-like (embryonal subtype) and associated with bleeding and ulceration.	Associated morphology	False	rabdomyosarkom iht. kategori	Inferred relationship	Some	2

Reference Sets

Concept inactivation indicator reference set

GB English

US English

REPLACED BY association reference set (foundation metadata concept)

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
1763601014	Rhabdomyosarcoma - category (morphologic abnormality)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1775923014	Rhabdomyosarcoma - category	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2763967014	Malignant soft tissue tumour of skeletal muscle differentiation	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2773622018	Malignant soft tissue tumor of skeletal muscle differentiation	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4533741000005115	rabdomyosarkom iht. kategori	da	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Danish module (core metadata concept)