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

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