FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

725138002: Perineal hemangioma, external genitalia malformation, lipomyelomeningocele, vesicorenal abnormality, imperforate anus syndrome (disorder)


Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3439336012 Perineal hemangioma, external genitalia malformation, lipomyelomeningocele, vesicorenal abnormality, imperforate anus syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3439337015 PELVIS syndrome en Synonym Active Case sensitive SNOMED CT core
3439338013 PELVIS (perineal hemangioma, external genitalia malformation, lipomyelomeningocele, vesicorenal abnormality, imperforate anus) syndrome en Synonym Active Case sensitive SNOMED CT core
3439339017 Perineal hemangioma, external genitalia malformation, lipomyelomeningocele, vesicorenal abnormality, imperforate anus syndrome en Synonym Active Case insensitive SNOMED CT core
3439340015 PELVIS (Perineal haemangioma, external genitalia malformation, lipomyelomeningocele, vesicorenal abnormality, imperforate anus) syndrome en Synonym Active Case sensitive SNOMED CT core
3439341016 Perineal haemangioma, external genitalia malformation, lipomyelomeningocele, vesicorenal abnormality, imperforate anus syndrome en Synonym Active Case insensitive SNOMED CT core
3439342011 PELVIS is an acronym defining the association of Perineal hemangioma, External genitalia malformations, Lipomyelomeningocele, Vesicorenal abnormalities, Imperforate anus and Skin tag. Eleven cases have been reported. en Definition Active Case sensitive SNOMED CT core
3439343018 PELVIS is an acronym defining the association of Perineal haemangioma, External genitalia malformations, Lipomyelomeningocele, Vesicorenal abnormalities, Imperforate anus and Skin tag. Eleven cases have been reported. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
PELVIS syndrome Finding site Blood vessel structure true Inferred relationship Some 1
PELVIS syndrome Occurrence Congenital true Inferred relationship Some 1
PELVIS syndrome Pathological process Pathological developmental process false Inferred relationship Some 1
PELVIS syndrome Associated morphology Benign haemangioma true Inferred relationship Some 1
PELVIS syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Some 2
PELVIS syndrome Pathological process Pathological developmental process true Inferred relationship Some 2
PELVIS syndrome Is a Multiple system malformation syndrome true Inferred relationship Some
PELVIS syndrome Is a Congenital haemangioma true Inferred relationship Some
PELVIS syndrome Occurrence Congenital true Inferred relationship Some 2
PELVIS syndrome Occurrence Congenital false Inferred relationship Some 3
PELVIS syndrome Associated morphology Benign haemangioma false Inferred relationship Some 2
PELVIS syndrome Finding site Blood vessel structure false Inferred relationship Some 2
PELVIS syndrome Associated morphology Developmental abnormality false Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Neoplasm and/or hamartoma reference set

Cardiovascular finding reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

Back to Start