FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

725905005: Infundibulopelvic stenosis multicystic kidney syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3446282017 Infundibulopelvic stenosis multicystic kidney syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3446283010 Infundibulopelvic stenosis multicystic kidney syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3446284016 Infundibulopelvic dysgenesis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3446282017 Infundibulopelvic stenosis multicystic kidney syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3446283010 Infundibulopelvic stenosis multicystic kidney syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3446284016 Infundibulopelvic dysgenesis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3446285015 A rare genetic renal malformation syndrome with characteristics of variable degrees of malformation in the pelvicalyceal system (including unilateral or bilateral calyceal dilatation, infundibular stenosis, hypoplasia or stenosis of the renal pelvis) which lead to multicystic kidney. Clinically it exhibits abdominal, lumbar or flank pain, recurrent urinary tract infections, hypertension, proteinuria and often progresses to renal insufficiency. Calyceal dilatation and hydronephrosis are frequently seen on imaging. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
913061000172113 syndrome de dysplasie rénale autosomique dominante-sténose infundibulo-pelvienne fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
913061000172113 syndrome de dysplasie rénale autosomique dominante-sténose infundibulo-pelvienne fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Infundibulopelvic stenosis multicystic kidney syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Infundibulopelvic stenosis multicystic kidney syndrome Is a Congenital anomaly of the kidney true Inferred relationship Existential restriction modifier (core metadata concept)
Infundibulopelvic stenosis multicystic kidney syndrome Is a Congenital anomaly of the urinary tract true Inferred relationship Existential restriction modifier (core metadata concept)
Infundibulopelvic stenosis multicystic kidney syndrome Is a Hereditary nephropathy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Infundibulopelvic stenosis multicystic kidney syndrome Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 1
Infundibulopelvic stenosis multicystic kidney syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Infundibulopelvic stenosis multicystic kidney syndrome Finding site Renal collecting system structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Infundibulopelvic stenosis multicystic kidney syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Infundibulopelvic stenosis multicystic kidney syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Infundibulopelvic stenosis multicystic kidney syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start