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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
Book syndrome Occurrence True Congenital Inferred relationship Some 3
Ballard syndrome Occurrence True Congenital Inferred relationship Some 2
Ballard syndrome Occurrence False Congenital Inferred relationship Some 3
Bamforth Lazarus syndrome Occurrence True Congenital Inferred relationship Some 3
Bamforth Lazarus syndrome Occurrence False Congenital Inferred relationship Some 4
Bamforth Lazarus syndrome Occurrence False Congenital Inferred relationship Some 5
Bartsocas Papas syndrome Occurrence True Congenital Inferred relationship Some 3
Bartsocas Papas syndrome Occurrence False Congenital Inferred relationship Some 4
Bartsocas Papas syndrome Occurrence False Congenital Inferred relationship Some 5
Congenital cataract with deafness and hypogonadism syndrome Occurrence False Congenital Inferred relationship Some 5
Congenital cataract with deafness and hypogonadism syndrome Occurrence False Congenital Inferred relationship Some 6
Congenital cataract with hypertrichosis and intellectual disability syndrome Occurrence False Congenital Inferred relationship Some 3
Congenital cataract with hypertrichosis and intellectual disability syndrome Occurrence False Congenital Inferred relationship Some 4
Congenital cataract with intellectual disability and hypogonadotropic hypogonadism syndrome Occurrence True Congenital Inferred relationship Some 3
Congenital cataract, nephropathy, encephalopathy syndrome Occurrence True Congenital Inferred relationship Some 3
Congenital cataract, nephropathy, encephalopathy syndrome Occurrence False Congenital Inferred relationship Some 4
Cataract and microcornea syndrome Occurrence True Congenital Inferred relationship Some 2
Cataract and microcornea syndrome Occurrence False Congenital Inferred relationship Some 3
Catel Manzke syndrome Occurrence True Congenital Inferred relationship Some 2
Catel Manzke syndrome Occurrence False Congenital Inferred relationship Some 3
CEDNIK syndrome Occurrence False Congenital Inferred relationship Some 5
CEDNIK syndrome Occurrence True Congenital Inferred relationship Some 6
CEDNIK syndrome Occurrence True Congenital Inferred relationship Some 7
Congenital hereditary facial paralysis with variable hearing loss syndrome Occurrence False Congenital Inferred relationship Some 6
Congenital hereditary facial paralysis with variable hearing loss syndrome Occurrence False Congenital Inferred relationship Some 7
Congenital intrauterine infection-like syndrome Occurrence True Congenital Inferred relationship Some 2
Congenital intrauterine infection-like syndrome Occurrence False Congenital Inferred relationship Some 3
Congenital lethal erythroderma Occurrence True Congenital Inferred relationship Some 1
Congenital malabsorptive diarrhoea due to paucity of enteroendocrine cells Occurrence True Congenital Inferred relationship Some 3
Ornithinaemia with gyrate atrophy Occurrence False Congenital Inferred relationship Some
Congenital absence of gastric muscle Occurrence True Congenital Inferred relationship Some 1
Congenital anomaly of mother complicating pregnancy Occurrence False Congenital Inferred relationship Some 1
Congenital chalasia of oesophagus Occurrence True Congenital Inferred relationship Some 1
Congenital short oesophagus Occurrence True Congenital Inferred relationship Some 1
Duplication cyst of oesophagus Occurrence True Congenital Inferred relationship Some 2
Duplication cyst of oesophagus Occurrence False Congenital Inferred relationship Some 3
Congenital infection caused by Echovirus Occurrence True Congenital Inferred relationship Some 1
Mucocutaneous early congenital syphilis Occurrence True Congenital Inferred relationship Some 1
Arteriovenous malformation of large intestine Occurrence False Congenital Inferred relationship Some 2
Arteriovenous malformation of large intestine Occurrence False Congenital Inferred relationship Some 3
Oculocutaneous albinism type 5 Occurrence False Congenital Inferred relationship Some 6
Oculocutaneous albinism type 6 Occurrence False Congenital Inferred relationship Some 6
Oculocutaneous albinism type 7 Occurrence False Congenital Inferred relationship Some 6
Odontoleukodystrophy Occurrence True Congenital Inferred relationship Some 2
Okamoto syndrome Occurrence False Congenital Inferred relationship Some 6
Congenital nephrotic syndrome due to congenital infection Occurrence True Congenital Inferred relationship Some 2
Congenital myogenic ptosis Occurrence False Congenital Inferred relationship Some
Ocular albinism with late-onset sensorineural deafness Occurrence False Congenital Inferred relationship Some 8
Oculogastrointestinal muscular dystrophy Occurrence True Congenital Inferred relationship Some 2
Oculogastrointestinal muscular dystrophy Occurrence False Congenital Inferred relationship Some 3
Omenn syndrome Occurrence True Congenital Inferred relationship Some 3
Glaucoma, ectopia, microspherophakia, stiff joint, short stature syndrome Occurrence False Congenital Inferred relationship Some 4
Gomez Lopez Hernandez syndrome Occurrence True Congenital Inferred relationship Some 4
Gomez Lopez Hernandez syndrome Occurrence False Congenital Inferred relationship Some 5
Gomez Lopez Hernandez syndrome Occurrence False Congenital Inferred relationship Some 6
Guttmacher syndrome Occurrence True Congenital Inferred relationship Some 4
Guttmacher syndrome Occurrence False Congenital Inferred relationship Some 5
Guttmacher syndrome Occurrence False Congenital Inferred relationship Some 6
Guttmacher syndrome Occurrence False Congenital Inferred relationship Some 7
Hennekam Beemer syndrome Occurrence False Congenital Inferred relationship Some 8
Hennekam Beemer syndrome Occurrence False Congenital Inferred relationship Some 9
Intellectual disability, craniofacial dysmorphism, hypogonadism, diabetes mellitus syndrome Occurrence True Congenital Inferred relationship Some 2
Intellectual disability, craniofacial dysmorphism, hypogonadism, diabetes mellitus syndrome Occurrence False Congenital Inferred relationship Some 3
Intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome Occurrence True Congenital Inferred relationship Some 3
Intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome Occurrence False Congenital Inferred relationship Some 4
Intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome Occurrence False Congenital Inferred relationship Some 5
Intellectual disability, developmental delay, contracture syndrome Occurrence False Congenital Inferred relationship Some 3
Intellectual disability, developmental delay, contracture syndrome Occurrence False Congenital Inferred relationship Some 4
Intellectual disability, developmental delay, contracture syndrome Occurrence False Congenital Inferred relationship Some 5
Juvenile cataract, microcornea, renal glucosuria syndrome Occurrence True Congenital Inferred relationship Some 3
Matthew Wood syndrome Occurrence True Congenital Inferred relationship Some 2
Matthew Wood syndrome Occurrence False Congenital Inferred relationship Some 3
Skeletal dysplasia with intellectual disability syndrome Occurrence False Congenital Inferred relationship Some 2
Von Voss-Cherstvoy syndrome Occurrence False Congenital Inferred relationship Some 7
Radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome Occurrence False Congenital Inferred relationship Some 5
Juvenile cataract, microcornea, renal glucosuria syndrome Occurrence False Congenital Inferred relationship Some 4
Ganglioside GM3 synthase deficiency Occurrence True Congenital Inferred relationship Some 2
Congenital keratoconus Occurrence True Congenital Inferred relationship Some 1
Congenital keratoconus posticus circumscriptus Occurrence True Congenital Inferred relationship Some 1
Sacral dysgenesis Occurrence True Congenital Inferred relationship Some 1
Deletion 5q35 Occurrence True Congenital Inferred relationship Some 2
Deletion 5q35 Occurrence True Congenital Inferred relationship Some 3
Early-onset X-linked optic atrophy Occurrence True Congenital Inferred relationship Some 2
Ectodermal dysplasia with blindness syndrome Occurrence True Congenital Inferred relationship Some 4
Ectodermal dysplasia with blindness syndrome Occurrence True Congenital Inferred relationship Some 5
Ectodermal dysplasia with blindness syndrome Occurrence False Congenital Inferred relationship Some 6
Ectodermal dysplasia with blindness syndrome Occurrence False Congenital Inferred relationship Some 7
Fuhrmann syndrome Occurrence True Congenital Inferred relationship Some 2
Fuhrmann syndrome Occurrence False Congenital Inferred relationship Some 3
Galloway Mowat syndrome Occurrence True Congenital Inferred relationship Some 2
Galloway Mowat syndrome Occurrence False Congenital Inferred relationship Some 3
GAPO syndrome Occurrence False Congenital Inferred relationship Some 6
GAPO syndrome Occurrence True Congenital Inferred relationship Some 7
Orofaciodigital syndrome type 10 Occurrence True Congenital Inferred relationship Some 4
Orofaciodigital syndrome type 10 Occurrence True Congenital Inferred relationship Some 5
Orofaciodigital syndrome type 10 Occurrence False Congenital Inferred relationship Some 6
Orofaciodigital syndrome type 10 Occurrence False Congenital Inferred relationship Some 7
Orofaciodigital syndrome type 5 Occurrence True Congenital Inferred relationship Some 4
Orofaciodigital syndrome type 5 Occurrence True Congenital Inferred relationship Some 5
Orofaciodigital syndrome type 5 Occurrence False Congenital Inferred relationship Some 6
Orofaciodigital syndrome type 5 Occurrence False Congenital Inferred relationship Some 7

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Reference Sets

Qualifier value foundation reference set

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