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1222666002: Ephrin receptor B4-related lymphatic-related hydrops fetalis (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-May 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5048396017 Ephrin receptor B4-related lymphatic-related hydrops fetalis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5048397014 Ephrin receptor B4-related lymphatic-related hydrops fetalis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5048398016 EPHB4-related lymphatic-related hydrops fetalis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5048401018 EPHB4-related generalised lymphatic dysplasia with non-immune hydrops fetalis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5048402013 EPHB4-related generalized lymphatic dysplasia with non-immune hydrops fetalis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5048403015 EPHB4-related generalised lymphatic dysplasia with atrial septal defect en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5048404014 EPHB4-related generalized lymphatic dysplasia with atrial septal defect en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399998016 A rare primary lymphedema characterized by a highly variable lymphatic phenotype ranging from severe lymphatic-related hydrops fetalis, which may cause perinatal demise or fully resolve to become completely asymptomatic, to a mild presentation in older patients with persistent varicose veins, peripheral edema, and impaired lymph drainage in the lower limbs. Atrial septal defect has been described in association and may be the only anomaly in some patients. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399999012 A rare primary lymphoedema characterised by a highly variable lymphatic phenotype ranging from severe lymphatic-related hydrops fetalis, which may cause perinatal demise or fully resolve to become completely asymptomatic, to a mild presentation in older patients with persistent varicose veins, peripheral oedema, and impaired lymph drainage in the lower limbs. Atrial septal defect has been described in association and may be the only anomaly in some patients. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5048396017 Ephrin receptor B4-related lymphatic-related hydrops fetalis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5048397014 Ephrin receptor B4-related lymphatic-related hydrops fetalis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5048398016 EPHB4-related lymphatic-related hydrops fetalis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5048401018 EPHB4-related generalised lymphatic dysplasia with non-immune hydrops fetalis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5048402013 EPHB4-related generalized lymphatic dysplasia with non-immune hydrops fetalis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5048403015 EPHB4-related generalised lymphatic dysplasia with atrial septal defect en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5048404014 EPHB4-related generalized lymphatic dysplasia with atrial septal defect en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5048399012 A rare primary lymphoedema characterised by a highly variable lymphatic phenotype ranging from severe lymphatic-related hydrops fetalis, which may cause perinatal demise or fully resolve to become completely asymptomatic, to a mild presentation in older patients with persistent varicose veins, peripheral oedema and impaired lymph drainage in the lower limbs. Atrial septal defect has been described in association and may be the only anomaly in some patients. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5048400017 A rare primary lymphedema characterized by a highly variable lymphatic phenotype ranging from severe lymphatic-related hydrops fetalis, which may cause perinatal demise or fully resolve to become completely asymptomatic, to a mild presentation in older patients with persistent varicose veins, peripheral edema and impaired lymph drainage in the lower limbs. Atrial septal defect has been described in association and may be the only anomaly in some patients. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399998016 A rare primary lymphedema characterized by a highly variable lymphatic phenotype ranging from severe lymphatic-related hydrops fetalis, which may cause perinatal demise or fully resolve to become completely asymptomatic, to a mild presentation in older patients with persistent varicose veins, peripheral edema, and impaired lymph drainage in the lower limbs. Atrial septal defect has been described in association and may be the only anomaly in some patients. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399999012 A rare primary lymphoedema characterised by a highly variable lymphatic phenotype ranging from severe lymphatic-related hydrops fetalis, which may cause perinatal demise or fully resolve to become completely asymptomatic, to a mild presentation in older patients with persistent varicose veins, peripheral oedema, and impaired lymph drainage in the lower limbs. Atrial septal defect has been described in association and may be the only anomaly in some patients. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3437811001000112 EPHB4-assoziierter fetaler Hydrops mit generalisierter lymphatischer Dysplasie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3437811001000112 EPHB4-assoziierter fetaler Hydrops mit generalisierter lymphatischer Dysplasie 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
EPHB4-related lymphatic-related hydrops fetalis Is a Primary lymphedema true Inferred relationship Existential restriction modifier (core metadata concept)
EPHB4-related lymphatic-related hydrops fetalis Is a Genetic disease true Inferred relationship Existential restriction modifier (core metadata concept)
EPHB4-related lymphatic-related hydrops fetalis Finding site Limb structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
EPHB4-related lymphatic-related hydrops fetalis Associated morphology Lymphatic edema true Inferred relationship Existential restriction modifier (core metadata concept) 1
EPHB4-related lymphatic-related hydrops fetalis Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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