105989001: Malformation sequence (disorder)

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

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

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

170408014 Malformation sequence en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

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 Only initial character 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

4740611000241111 séquence de malformation fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Malformation sequence	Is a	Multiple congenital malformations	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Malformation sequence	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Malformation sequence	Associated morphology	Congenital malformation	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Malformation sequence	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Malformation sequence	Is a	Congenital malformation syndrome	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Malformation sequence	Associated morphology	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Malformation sequence	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Malformation sequence	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Early urethral obstruction sequence (disorder)	Is a	False	Malformation sequence	Inferred relationship	Existential restriction modifier (core metadata concept)
Laterality sequence	Is a	True	Malformation sequence	Inferred relationship	Existential restriction modifier (core metadata concept)
Holoprosencephaly sequence	Is a	True	Malformation sequence	Inferred relationship	Existential restriction modifier (core metadata concept)
Athyrotic hypothyroidism sequence	Is a	True	Malformation sequence	Inferred relationship	Existential restriction modifier (core metadata concept)
Klippel-Feil sequence (disorder)	Is a	True	Malformation sequence	Inferred relationship	Existential restriction modifier (core metadata concept)
Exstrophy of urinary bladder sequence	Is a	True	Malformation sequence	Inferred relationship	Existential restriction modifier (core metadata concept)
Occult spinal dysraphism sequence	Is a	True	Malformation sequence	Inferred relationship	Existential restriction modifier (core metadata concept)
Allemann's syndrome (disorder)	Is a	True	Malformation sequence	Inferred relationship	Existential restriction modifier (core metadata concept)
Jugular lymphatic obstruction sequence	Is a	True	Malformation sequence	Inferred relationship	Existential restriction modifier (core metadata concept)
Septo-optic dysplasia sequence	Is a	False	Malformation sequence	Inferred relationship	Existential restriction modifier (core metadata concept)
syndrome de Di George	Is a	False	Malformation sequence	Inferred relationship	Existential restriction modifier (core metadata concept)
Caudal regression syndrome	Is a	True	Malformation sequence	Inferred relationship	Existential restriction modifier (core metadata concept)
Amniotic band syndrome	Is a	False	Malformation sequence	Inferred relationship	Existential restriction modifier (core metadata concept)
Immotile cilia syndrome	Is a	True	Malformation sequence	Inferred relationship	Existential restriction modifier (core metadata concept)
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	Existential restriction modifier (core metadata concept)
Sirenomelia sequence	Is a	False	Malformation sequence	Inferred relationship	Existential restriction modifier (core metadata concept)
Mayer-Rokitansky-Küster-Hauser syndrome type 2 (disorder)	Is a	False	Malformation sequence	Inferred relationship	Existential restriction modifier (core metadata concept)
Mayer Rokitansky Küster Hauser syndrome (disorder)	Is a	True	Malformation sequence	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets