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255399007: Congenital (qualifier value)

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

Descriptions:

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

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital Is a Periods of life true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Left atrioventricular valve dysplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Left atrioventricular valve hypoplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Left atrioventricular valve hypoplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Overriding left atrioventricular valve Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Overriding left atrioventricular valve Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Left atrioventricular valve leaflet abnormality Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Left atrioventricular valve leaflet abnormality Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Absent left atrioventricular valve leaflets Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Absent left atrioventricular valve leaflets Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Left atrioventricular valve prolapse Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Left atrioventricular valve prolapse Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Left atrioventricular valve leaflet dysplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Left atrioventricular valve leaflet dysplasia Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Abnormality of left atrioventricular valve chordae tendinae Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Abnormality of left atrioventricular valve chordae tendinae Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Congenital abnormality of left atrioventricular valve papillary muscle Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital fusion of left atrioventricular valve papillary muscles Occurrence False Congenital Inferred relationship Existential restriction modifier 3
Congenital hypoplastic left atrioventricular valve papillary muscle Occurrence False Congenital Inferred relationship Existential restriction modifier 3
Left atrioventricular valve stenosis in double inlet ventricle Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Left atrioventricular valve stenosis in double inlet ventricle Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Dilatation of left atrioventricular (not morphologically mitral) valve in double inlet ventricle Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Dilatation of left atrioventricular (not morphologically mitral) valve in double inlet ventricle Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Absent common atrioventricular valve papillary muscle Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Absent right atrioventricular valve leaflets Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital absence of right atrioventricular valve papillary muscle Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital glaucoma of left eye Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Lowry MacLean syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Spastic paraplegia, glaucoma, intellectual disability syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier 2
Congenital primary glaucoma of bilateral eyes Occurrence False Congenital Inferred relationship Existential restriction modifier 4
Microphthalmos due to Fryns syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Microphthalmos due to Delleman syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Micromelic dwarfism Fryn type Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital synostosis of bilateral tibias and fibulas Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Congenital split of bilateral feet Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Congenital split of bilateral hands Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Agenesis of metacarpal bone Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Dominant dystrophic epidermolysis bullosa with absence of skin Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Deletion of short arm of chromosome 18 Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Deletion of long arm of chromosome 18 Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Deletion of long arm of chromosome 13 Occurrence True Congenital Inferred relationship Existential restriction modifier 2
6q16 microdeletion syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 3
6q16 microdeletion syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 4
6q16 microdeletion syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 5
6q16 microdeletion syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 6
6q16 microdeletion syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 7
Uterus bicornis bicollis with blind hemi-vagina Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Uterus bicornis bicollis with blind hemi-vagina Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Uterus bicornis bicollis with patent cervix and vagina Occurrence True Congenital Inferred relationship Existential restriction modifier 2
External auditory canal atresia, vertical talus, hypertelorism syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 5
Congenital vertical talus deformity of bilateral ankles and feet Occurrence True Congenital Inferred relationship Existential restriction modifier 5
Pili torti Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Pili torti-deafness syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Complete phocomelia of bilateral lower limbs Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Complete phocomelia of bilateral lower limbs Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Complete phocomelia of bilateral lower limbs Occurrence True Congenital Inferred relationship Existential restriction modifier 5
Complete phocomelia of bilateral lower limbs Occurrence True Congenital Inferred relationship Existential restriction modifier 6
Complete phocomelia of bilateral lower limbs Occurrence True Congenital Inferred relationship Existential restriction modifier 7
Complete phocomelia of bilateral lower limbs Occurrence True Congenital Inferred relationship Existential restriction modifier 8
Complete phocomelia of lower limb Occurrence True Congenital Inferred relationship Existential restriction modifier 3
Complete phocomelia of lower limb Occurrence True Congenital Inferred relationship Existential restriction modifier 4
Rhizomelic chondrodysplasia punctata type 1 Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Rhizomelic chondrodysplasia punctata type 1 Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Proximal duplication of long arm of chromosome 5 Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Proximal duplication of long arm of chromosome 6 Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Renal tubular dysgenesis due to twin to twin transfusion Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Proximal duplication of long arm of chromosome 5 Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Proximal duplication of long arm of chromosome 6 Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Uniparental disomy of paternal origin of chromosome 4 Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Proximal duplication of long arm of chromosome 3 Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Proximal duplication of long arm of chromosome 4 Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Proximal duplication of long arm of chromosome 18 Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Proximal duplication of long arm of chromosome 2 Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Proximal duplication of long arm of chromosome 3 Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Proximal duplication of long arm of chromosome 4 Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Proximal duplication of long arm of chromosome 18 Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Proximal duplication of long arm of chromosome 2 Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Uniparental disomy of paternal origin of chromosome 15 Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Uniparental disomy of paternal origin of chromosome 14 Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Proximal duplication of long arm of chromosome 17 Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Uniparental disomy of paternal origin of chromosome 11 Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Proximal duplication of long arm of chromosome 17 Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Megalourethra of spongiose portion of urethra Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Proximal duplication of long arm of chromosome 12 Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Pfeiffer syndrome type 1 Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Pfeiffer syndrome type 1 Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Proximal duplication of long arm of chromosome 16 Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Proximal duplication of long arm of chromosome 10 Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Proximal duplication of long arm of chromosome 12 Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Proximal duplication of long arm of chromosome 16 Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Proximal duplication of long arm of chromosome 10 Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Mosaic 1q duplication Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Pelizaeus-Merzbacher disease in female carrier Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Pelizaeus-Merzbacher disease in female carrier Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Proximal duplication of short arm of chromosome 9 Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Pulverulent cataract Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Proximal duplication of short arm of chromosome 7 Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Proximal duplication of long arm of chromosome 11 Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Proximal duplication of short arm of chromosome 9 Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Proximal duplication of short arm of chromosome 7 Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Proximal duplication of long arm of chromosome 11 Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Proximal duplication of short arm of chromosome 8 Occurrence True Congenital Inferred relationship Existential restriction modifier 1

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