254819008: FAMM-syndroom (aandoening)

Descriptions:

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
B-K mole (nevus) syndrome	Is a	Dysplastic naevus of skin	true	Inferred relationship	Some
B-K mole (nevus) syndrome	Associated morphology	naevus naevocellularis - geen ICD-O-subtype (afwijkende morfologie)	false	Inferred relationship	Some	3
B-K mole (nevus) syndrome	Associated morphology	Neoplasm, benign	false	Inferred relationship	Some	3
B-K mole (nevus) syndrome	Pathological process	Neoplastic process	false	Inferred relationship	Some
B-K mole (nevus) syndrome	Pathological process	Benign neoplastic process	false	Inferred relationship	Some
B-K mole (nevus) syndrome	Finding site	Structure of skin region	false	Inferred relationship	Some	1
B-K mole (nevus) syndrome	Associated morphology	Melanocytic lesion morphology	false	Inferred relationship	Some	2
B-K mole (nevus) syndrome	Finding site	Skin structure	false	Inferred relationship	Some	2
B-K mole (nevus) syndrome	Is a	Multiple atypical melanocytic nevi (disorder)	false	Inferred relationship	Some
B-K mole (nevus) syndrome	Is a	Familial multiple tumor syndrome	false	Inferred relationship	Some
B-K mole (nevus) syndrome	Associated morphology	Dysplastic nevus	false	Inferred relationship	Some	1
B-K mole (nevus) syndrome	Associated morphology	congenitale anomalie (afwijkende morfologie)	false	Inferred relationship	Some
B-K mole (nevus) syndrome	Occurrence	Congenital	false	Inferred relationship	Some
B-K mole (nevus) syndrome	Finding site	Skin structure	false	Inferred relationship	Some	1
B-K mole (nevus) syndrome	Finding site	Skin structure	true	Inferred relationship	Some	1
B-K mole (nevus) syndrome	Associated morphology	Dysplastic nevus	true	Inferred relationship	Some	1
B-K mole (nevus) syndrome	Is a	Hereditary disorder of the integument	true	Inferred relationship	Some
B-K mole (nevus) syndrome	Occurrence	Period of life beginning after birth and ending before death (qualifier value)	false	Inferred relationship	Some	1
B-K mole (nevus) syndrome	Is a	Hereditary cancer-predisposing syndrome	true	Inferred relationship	Some

Inbound Relationships

Characteristic

Refinability

This concept is not in any reference sets

Id	Description	Lang	Type	Status	Case?	Module
379622012	FAMMM - Familial atypical mole malignant melanoma syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
379623019	Atypical mole syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
379624013	Familial atypical mole malignant melanoma syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
379625014	B-K mole (nevus) syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
645764010	Atypical mole syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
85001000146114	FAMM-syndroom	nl	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
728751000146111	FAMM-syndroom (aandoening)	nl	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
13300231000146112	erfelijk melanoom	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
13300241000146116	FAMMM-syndroom (familial atypical multiple mole melanoma syndrome); erfelijke afwijking(en) waardoor mensen een grotere kans hebben op een melanoom	nl	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)