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105989001: Malformation sequence (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
170408014 Malformation sequence en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
576992014 Malformation sequence (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4740611000241111 séquence de malformation fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

44 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Malformation sequence Is a Multiple congenital malformations false Inferred relationship Some
Malformation sequence Occurrence Congenital false Inferred relationship Some
Malformation sequence Associated morphology Congenital malformation false Inferred relationship Some
Malformation sequence Occurrence Congenital true Inferred relationship Some 1
Malformation sequence Is a Congenital malformation syndrome (disorder) true Inferred relationship Some
Malformation sequence Associated morphology anomalie du développement false Inferred relationship Some 1
Malformation sequence Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Malformation sequence Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Early urethral obstruction sequence Is a False Malformation sequence Inferred relationship Some
Laterality sequence Is a True Malformation sequence Inferred relationship Some
Holoprosencephaly sequence Is a True Malformation sequence Inferred relationship Some
Athyrotic hypothyroidism sequence Is a True Malformation sequence Inferred relationship Some
Klippel-Feil sequence Is a True Malformation sequence Inferred relationship Some
Exstrophy of urinary bladder sequence Is a True Malformation sequence Inferred relationship Some
Occult spinal dysraphism sequence Is a True Malformation sequence Inferred relationship Some
Allemann's syndrome (disorder) Is a True Malformation sequence Inferred relationship Some
Jugular lymphatic obstruction sequence Is a True Malformation sequence Inferred relationship Some
Septo-optic dysplasia sequence Is a False Malformation sequence Inferred relationship Some
syndrome de Di George Is a False Malformation sequence Inferred relationship Some
Caudal regression syndrome Is a True Malformation sequence Inferred relationship Some
Amniotic band syndrome Is a False Malformation sequence Inferred relationship Some
Immotile cilia syndrome Is a True Malformation sequence Inferred relationship Some
aplasie congénitale de l'utérus et des deux tiers supérieurs du vagin avec développement normal des caractères sexuels secondaires et caryotype normal Is a False Malformation sequence Inferred relationship Some
Sirenomelia sequence Is a False Malformation sequence Inferred relationship Some
Mayer-Rokitansky-Küster-Hauser syndrome type 2 (disorder) Is a False Malformation sequence Inferred relationship Some
A rare spectrum of Mullerian duct anomalies characterised by congenital aplasia of the uterus and upper two-thirds of the vagina in otherwise phenotypically normal females. It can be classified as either Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome type 1 (corresponding to isolated utero-vaginal aplasia) or MRKH syndrome type 2 (utero-vaginal aplasia associated with other malformations). Is a True Malformation sequence Inferred relationship Some

This concept is not in any reference sets

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