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

765750001: angio-osteohypotrofiesyndroom (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3659567013 Phlebectatic osteohypoplastic angiodysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3659568015 Angioosteohypotrophic syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3659569011 Servelle Martorell syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3659574015 Angio-osteohypotrophic syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3659575019 Angio-osteohypotrophic syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
7257211000146114 angio-osteohypotrofiesyndroom nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7257221000146116 angio-osteohypotrofiesyndroom (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7257231000146119 syndroom van Servelle-Martorell nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7257241000146110 flebectatische osteohypoplastische angiodysplasie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7257251000146113 Servelle-Martorell-syndroom nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3659570012 A rare congenital vascular anomaly syndrome characterised by venous or on occasion arterial malformations that lead to soft tissue hypertrophy and bone hypoplasia. An affected limb is generally shortened, highly deformed, painful and oedematous with associated bone and muscle hypotrophy. Single parts or multiple small parts of limbs are typically affected but more extensive involvement including complete extremity shoulder girdle and axilla have been reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3659571011 A rare congenital vascular anomaly syndrome characterized by venous or on occasion arterial malformations that lead to soft tissue hypertrophy and bone hypoplasia. An affected limb is generally shortened, highly deformed, painful and edematous with associated bone and muscle hypotrophy. Single parts or multiple small parts of limbs are typically affected but more extensive involvement including complete extremity shoulder girdle and axilla have been reported. 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
Angioosteohypotrophic syndrome Associated morphology Hypoplasia false Inferred relationship Some 1
Angioosteohypotrophic syndrome Occurrence Congenital true Inferred relationship Some 1
Angioosteohypotrophic syndrome Occurrence Congenital true Inferred relationship Some 2
Angioosteohypotrophic syndrome Is a Congenital vascular malformation (disorder) true Inferred relationship Some
Angioosteohypotrophic syndrome Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 2
Angioosteohypotrophic syndrome Finding site Bone structure false Inferred relationship Some 1
Angioosteohypotrophic syndrome Is a Congenital anomaly of skeletal bone true Inferred relationship Some
Angioosteohypotrophic syndrome Finding site Blood vessel structure (body structure) false Inferred relationship Some 2
Angioosteohypotrophic syndrome Associated morphology Hypoplasia true Inferred relationship Some 2
Angioosteohypotrophic syndrome Finding site Bone structure true Inferred relationship Some 2
Angioosteohypotrophic syndrome Finding site Blood vessel structure (body structure) true Inferred relationship Some 1
Angioosteohypotrophic syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Angioosteohypotrophic syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Angioosteohypotrophic syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start