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720636001: syndroom van cholestase met pigmentretinopathie en palatoschisis (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
3321615010 Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3321616011 Cholestasis with pigmentary retinopathy and cleft palate syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3321617019 Hardikar syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
6602201000146118 Hardikar-syndroom nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6602211000146116 syndroom van Hardikar nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6747831000146113 syndroom van cholestase met pigmentretinopathie en palatoschisis (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6747841000146117 syndroom van galstuwing met pigmentretinopathie en gespleten gehemelte nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6747851000146119 syndroom van cholestase met pigmentretinopathie en palatoschisis nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3321618012 A syndrome of multiple congenital malformations with an association of cleft lip and palate, patchy pigmentary retinopathy (cat's paw), obstructive liver disease (cholestasis, portal hypertension) and obstructive renal disease (ectopic ureteric insertion, obstruction, hydronephrosis). Gastrointestinal tract and cardiac involvement have also been reported. An overlap with Kabuki syndrome is debated. 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
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Finding site Urinary system structure (body structure) false Inferred relationship Some 9
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Is a Cholestasis true Inferred relationship Some
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Is a Cleft palate with cleft lip true Inferred relationship Some
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Is a Multiple system malformation syndrome true Inferred relationship Some
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Is a Congenital anomaly of liver true Inferred relationship Some
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Is a Retinal pigment deposits true Inferred relationship Some
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Is a Congenital malformation of the urinary system true Inferred relationship Some
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Associated morphology Congenital failure of fusion false Inferred relationship Some 6
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Occurrence Congenital false Inferred relationship Some 6
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Finding site Lip structure false Inferred relationship Some 6
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 7
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Occurrence Congenital false Inferred relationship Some 7
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Occurrence Congenital false Inferred relationship Some 8
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Occurrence Congenital false Inferred relationship Some 9
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Occurrence Congenital false Inferred relationship Some 10
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Associated morphology Congenital failure of fusion false Inferred relationship Some 8
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 9
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Associated morphology Deposition false Inferred relationship Some 10
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Finding site Retinal structure false Inferred relationship Some 10
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Finding site Liver structure false Inferred relationship Some 7
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Finding site Palatal structure false Inferred relationship Some 8
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Associated morphology Developmental failure of fusion (morphologic abnormality) false Inferred relationship Some 1
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Associated morphology Developmental failure of fusion (morphologic abnormality) false Inferred relationship Some 2
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Occurrence Congenital true Inferred relationship Some 2
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Finding site Lip structure false Inferred relationship Some 1
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Finding site Palatal structure false Inferred relationship Some 2
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 5
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Finding site Retinal structure true Inferred relationship Some 2
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Occurrence Congenital true Inferred relationship Some 3
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Associated morphology Deposition false Inferred relationship Some 2
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Associated morphology Developmental failure of fusion (morphologic abnormality) true Inferred relationship Some 3
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Occurrence Congenital true Inferred relationship Some 5
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Finding site Lip structure true Inferred relationship Some 3
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 5
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 4
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Occurrence Congenital true Inferred relationship Some 4
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Is a Congenital anomaly of retina true Inferred relationship Some
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Finding site Palatal structure true Inferred relationship Some 4
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Associated morphology Developmental failure of fusion (morphologic abnormality) true Inferred relationship Some 4
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Finding site Urinary system structure (body structure) true Inferred relationship Some 5
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Finding site Liver structure true Inferred relationship Some 1
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Associated morphology Pigment deposition true Inferred relationship Some 2
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Finding site Bone structure of head false Inferred relationship Some 6
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Pathological process (attribute) Pathological developmental process false Inferred relationship Some 6
Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder) Associated morphology Developmental failure of fusion (morphologic abnormality) false Inferred relationship Some 6

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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