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255399007: Congenital (qualifier value)

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
380598010 Congenital en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
380599019 Congenita en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
646433016 Congenital (qualifier value) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital Is a Periods of life false Inferred relationship Some
Congenital Is a Fetal and/or neonatal period true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Mandibuloacral dysostosis co-occurrent with type B lipodystrophy (disorder) Occurrence True Congenital Inferred relationship Some 4
Neuronal ceroid lipofuscinosis type 4 Occurrence True Congenital Inferred relationship Some 3
Neuronal ceroid lipofuscinosis type 8 Occurrence True Congenital Inferred relationship Some 2
Neuronal ceroid lipofuscinosis type 5 Occurrence True Congenital Inferred relationship Some 2
Neuronal ceroid lipofuscinosis type 6 (disorder) Occurrence True Congenital Inferred relationship Some 2
Neuronal ceroid lipofuscinosis type 7 Occurrence True Congenital Inferred relationship Some 2
Neuronal ceroid lipofuscinosis type 11 Occurrence True Congenital Inferred relationship Some 3
Neuronal ceroid lipofuscinosis type 13 Occurrence True Congenital Inferred relationship Some 2
Myoclonic disorder due to neuronal ceroid lipofuscinosis (disorder) Occurrence True Congenital Inferred relationship Some 4
Late-infantile neuronal ceroid lipofuscinosis Occurrence True Congenital Inferred relationship Some 1
Neuronal ceroid lipofuscinosis type 10 (disorder) Occurrence True Congenital Inferred relationship Some 4
Neuronal ceroid lipofuscinosis due to deficiency of cathepsin D (disorder) Occurrence True Congenital Inferred relationship Some 3
Neuronal ceroid lipofuscinosis type 3 Occurrence True Congenital Inferred relationship Some 2
Craniosynostosis, facial dysmorphism, Chiari-1 malformation, developmental and language delay syndrome Occurrence True Congenital Inferred relationship Some 1
Congenital deformity of breast Occurrence True Congenital Inferred relationship Some 1

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This concept is not in any reference sets

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