FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.24  |  FHIR Version n/a  User: [n/a]

721978002: syndroom van lymfoedeem, atriumseptumdefect en veranderingen in aangezicht (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3330009014 Lymphedema, atrial septal defect, facial changes syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3330010016 Lymphedema, atrial septal defect, facial changes syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3330011017 Lymphoedema, atrial septal defect, facial changes syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3330012012 Irons Bianchi syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
6729781000146110 syndroom van lymfoedeem, atriumseptumdefect en veranderingen in aangezicht nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6729791000146112 syndroom van lymfoedeem, atriumseptumdefect en veranderingen in aangezicht (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6850331000146115 syndroom van Irons-Bianchi nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6850341000146111 syndroom van Irons-Bhan nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7003111000146113 syndroom van lymfoedeem, atriumseptumdefect en veranderingen in gelaat nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3330013019 This syndrome is characterized by congenital lymphedema of the lower limbs, atrial septal defect and a characteristic facies (a round face with a prominent forehead, a flat nasal bridge with a broad nasal tip, epicanthal folds, a thin upper lip and a cleft chin). It has been described in two brothers and a sister. Transmission appears to be autosomal recessive. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3330014013 This syndrome is characterised by congenital lymphoedema of the lower limbs, atrial septal defect and a characteristic facies (a round face with a prominent forehead, a flat nasal bridge with a broad nasal tip, epicanthal folds, a thin upper lip and a cleft chin). It has been described in two brothers and a sister. Transmission appears to be autosomal recessive. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Is a Congenital septal defect of heart false Inferred relationship Some
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Some
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Is a Hereditary lymphedema false Inferred relationship Some
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Is a Cardiovascular system hereditary disorder true Inferred relationship Some
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Is a Lymphedema of lower extremity (disorder) false Inferred relationship Some
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Is a Congenital abnormality of atrial septum (disorder) false Inferred relationship Some
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 3
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Occurrence Congenital true Inferred relationship Some 3
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Finding site Face structure false Inferred relationship Some 3
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Associated morphology Congenital septal defect (morphologic abnormality) false Inferred relationship Some 4
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Occurrence Congenital false Inferred relationship Some 4
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Finding site Interatrial septum structure false Inferred relationship Some 4
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Associated morphology Lymphatic edema false Inferred relationship Some 5
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Occurrence Congenital false Inferred relationship Some 5
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Finding site Lower limb structure false Inferred relationship Some 5
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Associated morphology Lymphatic edema true Inferred relationship Some 3
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Finding site Lower limb structure true Inferred relationship Some 3
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Is a Congenital abnormality of cardiac connection false Inferred relationship Some
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Is a Congenital atrial septal defect (disorder) true Inferred relationship Some
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Is a Congenital anomaly of lower limb (disorder) true Inferred relationship Some
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Occurrence Congenital true Inferred relationship Some 2
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Finding site Interatrial septum structure true Inferred relationship Some 1
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 2
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Associated morphology Congenital septal defect (morphologic abnormality) true Inferred relationship Some 1
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Finding site Face structure true Inferred relationship Some 2
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Is a Developmental hereditary disorder false Inferred relationship Some
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Is a Congenital anomaly of heart septum false Inferred relationship Some
Lymphedema, atrial septal defect, facial changes syndrome (disorder) Is a Hereditary lymphedema of lower extremity (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start