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19886006: Sturge-Weber syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
33470014 Sturge-Weber sequence en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
33471013 Encephalotrigeminal angiomatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
33472018 Sturge-Kalischer-Weber syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
33473011 Sturge-Weber syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
33474017 Sturge-Weber disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1216099019 Encephalofacial haemangiomatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1217604010 Encephalofacial hemangiomatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1222364012 Sturge-Weber-Dimitri syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1222365013 Angiomatosis oculo-orbital-thalamo-encephalic syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1222366014 Encephalocutaneous angiomatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1222367017 Neuroretinoangiomatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2788206015 Sturge-Weber syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
33470014 Sturge-Weber sequence en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
33471013 Encephalotrigeminal angiomatosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
33471013 Encephalotrigeminal angiomatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
33472018 Sturge-Kalischer-Weber syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
33473011 Sturge-Weber syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
33474017 Sturge-Weber disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
748493011 Sturge-Weber sequence (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
748493011 Sturge-Weber sequence (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
1216099019 Encephalofacial haemangiomatosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1216099019 Encephalofacial haemangiomatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1217604010 Encephalofacial hemangiomatosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1217604010 Encephalofacial hemangiomatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1222364012 Sturge-Weber-Dimitri syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1222364012 Sturge-Weber-Dimitri syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1222365013 Angiomatosis oculo-orbital-thalamo-encephalic syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1222365013 Angiomatosis oculo-orbital-thalamo-encephalic syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1222366014 Encephalocutaneous angiomatosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1222366014 Encephalocutaneous angiomatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1222367017 Neuroretinoangiomatosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1222367017 Neuroretinoangiomatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2788206015 Sturge-Weber syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3416341001000113 Sturge-Weber-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
939641000172113 angiomatose de Sturge-Weber-Krabbe fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
971631000172116 syndrome de Sturge-Weber fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
939641000172113 angiomatose de Sturge-Weber-Krabbe fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
971631000172116 syndrome de Sturge-Weber fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3416341001000113 Sturge-Weber-Syndrom 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
Sturge-Weber syndrome (disorder) Is a Port-wine stain of skin false Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Is a Neoplasm of blood vessel of face false Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Is a Cardiovascular system hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Is a Neoplasm of central nervous system false Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Is a Neoplasm of skin of face (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Is a Disorder of skin AND/OR subcutaneous tissue of head (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Is a Neurocutaneous syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Is a Congenital anomaly of face false Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Sturge-Weber syndrome (disorder) Pathological process Benign neoplastic process false Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Finding site Cardiovascular system subdivision false Inferred relationship Existential restriction modifier (core metadata concept) 2
Sturge-Weber syndrome (disorder) Associated morphology Angiomatosis false Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Finding site Structure of central nervous system false Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Associated morphology Dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Sturge-Weber syndrome (disorder) Associated morphology Neoplasm, benign false Inferred relationship Existential restriction modifier (core metadata concept) 3
Sturge-Weber syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Finding site Structure of capillary blood vessel false Inferred relationship Existential restriction modifier (core metadata concept) 1
Sturge-Weber syndrome (disorder) Associated morphology Vascular naevus false Inferred relationship Existential restriction modifier (core metadata concept) 4
Sturge-Weber syndrome (disorder) Finding site Structure of skin region (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Sturge-Weber syndrome (disorder) Finding site Structure of skin region (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Sturge-Weber syndrome (disorder) Pathological process Neoplastic process false Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Finding site Skin of part of face (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Finding site Venous structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Sturge-Weber syndrome (disorder) Is a néoplasme bénin de la tête et du cou false Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Finding site Structure of skin region (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Sturge-Weber syndrome (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 4
Sturge-Weber syndrome (disorder) Finding site Blood vessel structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Sturge-Weber syndrome (disorder) Finding site Skin of face false Inferred relationship Existential restriction modifier (core metadata concept) 3
Sturge-Weber syndrome (disorder) Is a Disorder of the central nervous system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Is a Benign neoplasm of skin of face true Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Associated morphology Dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 3
Sturge-Weber syndrome (disorder) Associated morphology Dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Sturge-Weber syndrome (disorder) Is a Venous malformation false Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Is a Vascular hamartoma of skin false Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Is a Hamartomatous disease false Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Is a Congenital anomaly of head false Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Associated morphology Congenital capillary proliferation false Inferred relationship Existential restriction modifier (core metadata concept) 4
Sturge-Weber syndrome (disorder) Finding site Structure of capillary of skin false Inferred relationship Existential restriction modifier (core metadata concept) 4
Sturge-Weber syndrome (disorder) Associated morphology Hamartoma false Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Associated morphology Dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Sturge-Weber syndrome (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Sturge-Weber syndrome (disorder) Is a Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Finding site Nervous system structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Sturge-Weber syndrome (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Sturge-Weber syndrome (disorder) Associated morphology Congenital vascular anomaly false Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Sturge-Weber syndrome (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Sturge-Weber syndrome (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Sturge-Weber syndrome (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Sturge-Weber syndrome (disorder) Is a Congenital vascular malformation (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Is a Cardiovascular system hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Finding site Blood vessel structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Sturge-Weber syndrome (disorder) Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept) 2
Sturge-Weber syndrome (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Sturge-Weber syndrome (disorder) Finding site Nervous system structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Sturge-Weber syndrome (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Sturge-Weber syndrome (disorder) Finding site Blood vessel structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Sturge-Weber syndrome (disorder) Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept) 2
Sturge-Weber syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
Sturge-Weber syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 4
Sturge-Weber syndrome (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 4
Sturge-Weber syndrome (disorder) Finding site Nervous system structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 4
Sturge-Weber syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 5
Sturge-Weber syndrome (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 5
Sturge-Weber syndrome (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Sturge-Weber syndrome (disorder) Finding site Nervous system structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 5
Sturge-Weber syndrome (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 4
Sturge-Weber syndrome (disorder) Is a Congenital hamartoma (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Associated morphology Hamartoma false Inferred relationship Existential restriction modifier (core metadata concept) 3
Sturge-Weber syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 6
Sturge-Weber syndrome (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 6
Sturge-Weber syndrome (disorder) Finding site Blood vessel structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 6
Sturge-Weber syndrome (disorder) Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Sturge-Weber syndrome (disorder) Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 4
Sturge-Weber syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Sturge-Weber syndrome (disorder) Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Sturge-Weber syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Sturge-Weber syndrome (disorder) Associated morphology Hamartoma false Inferred relationship Existential restriction modifier (core metadata concept) 2
Sturge-Weber syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 4
Sturge-Weber syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Sturge-Weber syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 3
Sturge-Weber syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Sturge-Weber syndrome (disorder) Is a Congenital leptomeningeal angiomatosis true Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Is a Hemangioma of face (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Is a Mass of skin of head (finding) false Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Is a Haemangioma of skin and subcutaneous tissue true Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Is a Lesion of skin of face false Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Associated morphology Angiomatosis true Inferred relationship Existential restriction modifier (core metadata concept) 1
Sturge-Weber syndrome (disorder) Finding site Leptomeninges structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Sturge-Weber syndrome (disorder) Associated morphology Capillary haemangioma true Inferred relationship Existential restriction modifier (core metadata concept) 2
Sturge-Weber syndrome (disorder) Finding site Skin of face true Inferred relationship Existential restriction modifier (core metadata concept) 2
Sturge-Weber syndrome (disorder) Finding site Nervous system structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Sturge-Weber syndrome (disorder) Associated morphology Neoplasm true Inferred relationship Existential restriction modifier (core metadata concept) 3
Sturge-Weber syndrome (disorder) Associated morphology Neoplasm false Inferred relationship Existential restriction modifier (core metadata concept) 4
Sturge-Weber syndrome (disorder) Is a Vascular neoplasm of skin (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Sturge-Weber syndrome (disorder) Is a Benign neoplasm of blood vessel true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Gingival enlargement due to Sturge-Weber syndrome Due to True Sturge-Weber syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept) 2

This concept is not in any reference sets

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