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66091009: Congenital disease (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
109766011 Congenital disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
500308011 Congenital disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
805666017 Congenital disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
109766011 Congenital disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
109766011 Congenital disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
500308011 Congenital disorder en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
500308011 Congenital disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
500309015 Congenital abnormality en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
500310013 Fetal developmental abnormality en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
805666017 Congenital disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
805666017 Congenital disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3011638011 Foetal developmental abnormality en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3921000077116 maladie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
10211000188115 pathologie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3921000077116 maladie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
10211000188115 pathologie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

10200 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital disease Is a Disease false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital disease Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital disease Is a Disorder of foetus and/or newborn true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
anomalie congénitale régionale Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital malformation Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital deformity (disorder) Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Embryological remnant Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
structure dysmorphique Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital immunodeficiency disease Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of integument Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of neck Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of the haematopoietic system Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
anomalies fœtales congénitales Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of digestive system Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of musculoskeletal system Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital chromosomal disease Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Hamartomatous disease Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
anomalie congénitale de l'appareil respiratoire Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of trunk Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital infectious disease Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Inborn error of metabolism Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of head Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of nervous system Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of animal tail Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of cardiovascular system Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Ear, face and neck congenital anomalies (disorder) Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Other specified face and neck anomalies Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Other specified nonteratogenic anomalies Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Unspecified anomaly of connective tissue Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Other specified integument anomaly Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Other and unspecified congenital anomalies Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Monster NOS Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
[X]Additional congenital disease classification terms Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
[X]Other specified congenital malformations of integument Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Integument anomalies NOS Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Other congenital anomalies Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Central nervous system (SNC)/head/neck congenital anomaly NOS Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Family history of congenital disease (situation) Associated finding False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of anencephaly Associated finding False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Family history: Congenital anomaly NOS Associated finding False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital meningocele Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Myofibromatosis Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital malformation of tongue, mouth and pharynx Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital functional disorders of the small intestine Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of the thymus (disorder) Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of endocrine gland Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of limb Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Abnormal umbilical cord (disorder) Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
myasthénie congénitale et du développement Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Abdominal wall anomalies Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital obstruction of ureteropelvic junction Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Family history: Congenital gastrointestinal tract anomaly (situation) Associated finding False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Family history: Congenital genitourinary anomaly (situation) Associated finding False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital eye disorder screening (procedure) Has focus False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Infantile myofibromatosis Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly - oral/respiratory Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hamartoma (disorder) Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Nicolaides-Baraitser syndrome Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital malignant melanoma (disorder) Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypothyroidism (disorder) Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
hyperplasie corticosurrénale congénitale Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital vaginal enterocele Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypertonia Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Generalized failure of tooth eruption associated with systemic disease Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital auditory imperception Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital disorder of facial nerve Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital myasthenic syndrome (disorder) Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital end-plate acetylcholinesterase deficiency (disorder) Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital and developmental anomalies of the nervous system Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital pseudobulbar palsy Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital dysphasia Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Infantile esotropia (disorder) Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital vocal cord palsy Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital factor IX deficiency variant Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital factor IX deficiency with inhibitor Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
maladie de von Willebrand congénitale Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital fibrinogen abnormality Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital microvillous atrophy Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Pericellular fibrosis of congenital syphilis Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Pulmonic stenosis and congenital nephrosis Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital male infertility Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital adrenal hyperplasia Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Extensive congenital erosions, vesicles and reticulate scarring Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital myotonic dystrophy Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital OR acquired abnormality of cervix affecting pregnancy Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital OR acquired abnormality of vagina affecting pregnancy Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital OR acquired abnormality of vulva affecting pregnancy Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Malignant melanoma arising in congenital nevus Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Hydrocephalus associated with congenital aqueduct stenosis (disorder) Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital exotropia Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital primary adrenocortical hypofunction (disorder) Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital sensory neuropathy with selective loss of small myelinated fibres Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital heart disease (disorder) Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of eye Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital myotonia, autosomal recessive form Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital secretory diarrhoea Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Ectopic placenta Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
malabsorption congénitale du glucose-galactose Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital fecaliths Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Pituitary dwarfism Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Metachromatic leukodystrophy, congenital type Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Abnormal tooth eruption Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital lactase deficiency Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital myotonia, autosomal dominant form Is a False Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)

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