105989001: Malformation sequence (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\...

\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital malformation syndrome (disorder)\Malformation sequence

\Developmental disorder\Congenital malformation\Congenital malformation syndrome (disorder)\Malformation sequence

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

2014441000005111 Misdannelsessekvens da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Malformation sequence	Is a	Multiple kongenitte misdannelser	false	Inferred relationship	Some
Malformation sequence	Occurrence	Congenital	false	Inferred relationship	Some
Malformation sequence	Associated morphology	Kongenit 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	dysgenese	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 (disorder)	Is a	False	Malformation sequence	Inferred relationship	Some
DiGeorges syndrom	Is a	False	Malformation sequence	Inferred relationship	Some
Caudal regression syndrome	Is a	True	Malformation sequence	Inferred relationship	Some
Afklemningssyndrom	Is a	False	Malformation sequence	Inferred relationship	Some
Immotile cilia syndrome	Is a	True	Malformation sequence	Inferred relationship	Some
Rokitanskys sekvens	Is a	False	Malformation sequence	Inferred relationship	Some
Sirenomeli-sekvens	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