255399007: Congenital (qualifier value)

SNOMED CT Concept\Qualifier value\...

\Precondition value (qualifier value)\Periods of life\Congenital

\Special atomic mapping values\Special disorder atoms\Temporal periods\Periods of life\Congenital

\Descriptor (qualifier value)\Time patterns\Temporal periods\Periods of life\Congenital

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

Descriptions:

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
Linear/nevoid/zosteriform Darier's disease (disorder)	Occurrence	False	Congenital	Inferred relationship	Some	2
Mandibular prognathism	Occurrence	False	Congenital	Inferred relationship	Some	1
Microcephaly, microphthalmia, ectrodactyly of lower limbs and prognathism syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
Fanconi's anemia	Occurrence	True	Congenital	Inferred relationship	Some	4
Autosomal recessive congenital methemoglobinemia (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Autosomal recessive congenital methaemoglobinaemia type II	Occurrence	True	Congenital	Inferred relationship	Some	1
Autosomal recessive congenital methemoglobinemia type I	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital talipes calcaneovalgus	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital conjunctival cyst	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital cyst of posterior segment of eye	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital cyst of esophagus	Occurrence	True	Congenital	Inferred relationship	Some	1
Hypotrichosis with keratosis pilaris and lentiginosis	Occurrence	False	Congenital	Inferred relationship	Some	1
Cyst of Wolffian duct	Occurrence	True	Congenital	Inferred relationship	Some	1
Peutz-Jeghers syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
Peutz-Jeghers syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Embryonic cyst of Gartner's duct	Occurrence	True	Congenital	Inferred relationship	Some	1
Manus valga	Occurrence	True	Congenital	Inferred relationship	Some	1
Wolffian duct cyst - male	Occurrence	True	Congenital	Inferred relationship	Some	1
Familial generalised lentiginosis	Occurrence	True	Congenital	Inferred relationship	Some	1
Wolffian duct cyst - female	Occurrence	True	Congenital	Inferred relationship	Some	1
Peutz-Jeghers polyps of small bowel	Occurrence	True	Congenital	Inferred relationship	Some	2
Peutz-Jeghers polyps of small bowel	Occurrence	True	Congenital	Inferred relationship	Some	3
Arterial dissection and lentiginosis syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Embryonic cyst of female genital structure	Occurrence	True	Congenital	Inferred relationship	Some	1
Embryonic cyst of male genital structure (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Manus vara	Occurrence	True	Congenital	Inferred relationship	Some	1
Embryonic cyst of epoophoron	Occurrence	True	Congenital	Inferred relationship	Some	1
Reticulate acropigmentation of Kitamura	Occurrence	True	Congenital	Inferred relationship	Some	1
Centrofacial lentiginosis syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Embryonic cyst of vagina (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Cyst of paramesonephric duct (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Keratosis follicularis, dwarfism, cerebral atrophy syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
förvärvad abnormitet i atrioventrikulärklaff, inte morfologiskt mitral eller trikuspidal, associerad med atrioventrikulär septumdefekt	Occurrence	False	Congenital	Inferred relationship	Some	2
Factor XI deficiency, type I	Occurrence	True	Congenital	Inferred relationship	Some	2
Odontogenic keratocyst	Occurrence	True	Congenital	Inferred relationship	Some	1
Hereditary factor IX deficiency disease with inhibitor (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Naso-labial cyst	Occurrence	True	Congenital	Inferred relationship	Some	1
Non-odontogenic developmental cyst of jaw	Occurrence	True	Congenital	Inferred relationship	Some	1
Buccal bifurcation cyst	Occurrence	True	Congenital	Inferred relationship	Some	1
Hereditary factor IX deficiency disease	Occurrence	True	Congenital	Inferred relationship	Some	1
Median palatal cyst	Occurrence	True	Congenital	Inferred relationship	Some	1
Moderate hereditary factor IX deficiency disease without inhibitor (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Odontogenic cyst	Occurrence	False	Congenital	Inferred relationship	Some	1
Severe hereditary factor IX deficiency disease without inhibitor (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Gingival cyst of adult	Occurrence	True	Congenital	Inferred relationship	Some	1
Mild hereditary factor IX deficiency disease without inhibitor (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Cervical spinal meningocele	Occurrence	True	Congenital	Inferred relationship	Some	1
Botryoid odontogenic cyst (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Moderate hereditary factor IX deficiency disease with inhibitor (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Lumbar spinal meningocele (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Mild hereditary factor IX deficiency disease with inhibitor (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
medfött spinalt hydromeningocele	Occurrence	False	Congenital	Inferred relationship	Some	2
Naso-palatine duct cyst	Occurrence	True	Congenital	Inferred relationship	Some	1
Lipomeningocele	Occurrence	True	Congenital	Inferred relationship	Some	3
Gingival cyst of neonate (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
kranialt hydromeningocele	Occurrence	False	Congenital	Inferred relationship	Some	4
Dentigerous cyst	Occurrence	True	Congenital	Inferred relationship	Some	1
Lateral meningocele	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital cerebral meningocele	Occurrence	False	Congenital	Inferred relationship	Some	3
Severe hereditary factor IX deficiency disease with inhibitor (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Factor XI deficiency, type II	Occurrence	True	Congenital	Inferred relationship	Some	2
Extraosseous calcifying odontogenic cyst	Occurrence	True	Congenital	Inferred relationship	Some	1
Factor XI deficiency, type III	Occurrence	True	Congenital	Inferred relationship	Some	2
Median mandibular cyst	Occurrence	True	Congenital	Inferred relationship	Some	1
främre mediancysta i överkäken	Occurrence	False	Congenital	Inferred relationship	Some	1
Congenital meningocele	Occurrence	True	Congenital	Inferred relationship	Some	1
Hereditary factor XI deficiency disease	Occurrence	True	Congenital	Inferred relationship	Some	1
Hereditary factor IX deficiency disease without inhibitor (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Globulo-maxillary cyst	Occurrence	True	Congenital	Inferred relationship	Some	1
Lateral radicular cyst	Occurrence	False	Congenital	Inferred relationship	Some	1
Embryonic cyst of omentum (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Glandular odontogenic cyst	Occurrence	True	Congenital	Inferred relationship	Some	1
Residual cyst	Occurrence	False	Congenital	Inferred relationship	Some	1
Eruption cyst of jaw (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Inflammatory odontogenic cyst	Occurrence	False	Congenital	Inferred relationship	Some	1
Primordial cyst	Occurrence	True	Congenital	Inferred relationship	Some	1
Lateral developmental cyst of jaw	Occurrence	True	Congenital	Inferred relationship	Some	1
Radicular cyst	Occurrence	False	Congenital	Inferred relationship	Some	1
Thoracic spinal meningocele	Occurrence	True	Congenital	Inferred relationship	Some	1
Secondary megacolon - congenital	Occurrence	True	Congenital	Inferred relationship	Some	1
Branchial cleft cyst	Occurrence	True	Congenital	Inferred relationship	Some	1
16p12.2 microdeletion syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
16p12.2 microdeletion syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
5q31.3 microdeletion syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
5q31.3 microdeletion syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
5q31.3 microdeletion syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	3
X-bunden akrogigantism	Occurrence	False	Congenital	Inferred relationship	Some	2
X-bunden akrogigantism	Occurrence	False	Congenital	Inferred relationship	Some	1
15q13.3 microduplication syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Congenital secondary hydronephrosis (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Primary tethered cord syndrome	Occurrence	True	Congenital	Inferred relationship	Some	2
Primary tethered cord syndrome	Occurrence	True	Congenital	Inferred relationship	Some	1
Primary tethered cord syndrome	Occurrence	True	Congenital	Inferred relationship	Some	3
Primary tethered cord syndrome	Occurrence	True	Congenital	Inferred relationship	Some	4
Coloboma of retina	Occurrence	True	Congenital	Inferred relationship	Some	1
Tall stature, intellectual disability, facial dysmorphism syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
N-glycanase 1 congenital disorder of deglycosylation (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Trisomy 1q syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	1
Trisomy 1q syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2
Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	5
Trisomy 8p syndrome (disorder)	Occurrence	True	Congenital	Inferred relationship	Some	2

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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
135131000052119	medfödd	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)