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255399007: Congenital (qualifier value)

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
380598010 Congenital en Synonym Active Case insensitive SNOMED CT core
380599019 Congenita en Synonym Active Case insensitive SNOMED CT core
646433016 Congenital (qualifier value) en Fully specified name Active Case insensitive SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital Is a Periods of life true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Spondylodysplasia Occurrence False Congenital Inferred relationship Some
Short rib dysplasia Occurrence False Congenital Inferred relationship Some
Atelosteogenesis/diastrophic dysplasia Occurrence False Congenital Inferred relationship Some
Kniest-Stickler dysplasia Occurrence False Congenital Inferred relationship Some
Dysostosis multiplex Occurrence False Congenital Inferred relationship Some
Furst-Ostrum syndrome Occurrence False Congenital Inferred relationship Some
Bent bone dysplasia Occurrence False Congenital Inferred relationship Some
Pseudochondroplasia Occurrence False Congenital Inferred relationship Some
Congenital ectodermal defect Occurrence False Congenital Inferred relationship Some
Congenital ichthyosiform erythroderma Occurrence True Congenital Inferred relationship Some 3
Bullous rash of hand Occurrence False Congenital Inferred relationship Some
Progressive recessive dystrophic epidermolysis bullosa Occurrence False Congenital Inferred relationship Some
Generalised epidermolysis bullosa simplex Occurrence False Congenital Inferred relationship Some
Congenital non-neoplastic naevus Occurrence False Congenital Inferred relationship Some
Hereditary acantholytic dermatosis Occurrence False Congenital Inferred relationship Some
Segmental neurofibromatosis Occurrence False Congenital Inferred relationship Some
Diffuse neurofibroma Occurrence False Congenital Inferred relationship Some
Congenital malformation syndrome due to known exogenous cause Occurrence False Congenital Inferred relationship Some
Absence of sex chromosome Occurrence False Congenital Inferred relationship Some
Pseudotrisomy 18 Occurrence False Congenital Inferred relationship Some
Autosomal deletion - mosaicism Occurrence False Congenital Inferred relationship Some
Turner's phenotype, partial X deletion karyotype Occurrence False Congenital Inferred relationship Some
Arteriovenous malformation of skin Occurrence False Congenital Inferred relationship Some

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Reference Sets

Qualifier value foundation reference set

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