154481000146109: X-gebonden dominante erytropoëtische protoporfyrie (aandoening)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2022. Module: SNOMED CT Netherlands NRC maintained module (core metadata concept)

Descriptions:

Id Description Lang Type Status Case? Module

12991581000146115 X-linked dominant erythropoietic protoporphyria (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

12991591000146118 X-linked dominant erythropoietic protoporphyria en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

12991601000146111 XLDPP en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

12999451000146110 X-gebonden dominante erytropoëtische protoporfyrie nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

12999461000146113 X-gebonden dominante erytropoëtische protoporfyrie (aandoening) nl Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

13673021000146111 XLDPP nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
X-gebonden dominante erytropoëtische protoporfyrie	Is a	X-linked hereditary disease	false	Inferred relationship	Some
X-gebonden dominante erytropoëtische protoporfyrie	Is a	Ferrochelatase deficiency	false	Inferred relationship	Some
X-gebonden dominante erytropoëtische protoporfyrie	Occurrence	Congenital	false	Inferred relationship	Some	1
X-gebonden dominante erytropoëtische protoporfyrie	Is a	Congenital porphyria	false	Inferred relationship	Some
X-gebonden dominante erytropoëtische protoporfyrie	Is a	Inborn error of metabolism	false	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Concept inactivation indicator reference set

SAME AS association reference set (foundation metadata concept)