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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
Salla disease Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital urethrorectal fistula Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital cystic lung Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital subaortic stenosis due to fibromuscular shelf Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of appendix Occurrence False Congenital Inferred relationship Existential restriction modifier
Hyperplasia of islet alpha cells with glucagon excess Occurrence False Congenital Inferred relationship Existential restriction modifier
Persistent convolutions of aortic arch Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of head Occurrence False Congenital Inferred relationship Existential restriction modifier
Supernumerary vertebra Occurrence False Congenital Inferred relationship Existential restriction modifier
Monorchism Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital syphilis with gumma Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of vagina Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital fistula of salivary gland Occurrence False Congenital Inferred relationship Existential restriction modifier
Acquired equinovarus deformity Occurrence False Congenital Inferred relationship Existential restriction modifier
Hyperplastic chondrodystrophy Occurrence False Congenital Inferred relationship Existential restriction modifier
Ectopic gallbladder Occurrence False Congenital Inferred relationship Existential restriction modifier
Hecht syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Pelizaeus-Merzbacher disease, classic form Occurrence False Congenital Inferred relationship Existential restriction modifier 4
Acquired pharyngoesophageal diverticulum Occurrence False Congenital Inferred relationship Existential restriction modifier
Pyruvate carboxylase deficiency Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Isovaleryl-coenzyme A dehydrogenase deficiency Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Buphthalmos with congenital keratoglobus Occurrence False Congenital Inferred relationship Existential restriction modifier
Rokitansky sequence Occurrence False Congenital Inferred relationship Existential restriction modifier
Cleft palate Occurrence False Congenital Inferred relationship Existential restriction modifier
Female pseudohermaphroditism Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital cranial osteoporosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital megalogastria Occurrence False Congenital Inferred relationship Existential restriction modifier
Biotinidase deficiency Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Nodular renal blastema Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital onychauxis Occurrence False Congenital Inferred relationship Existential restriction modifier
Ring chromosome 18 syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Pachydermoperiostosis syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital stenosis of vena cava Occurrence False Congenital Inferred relationship Existential restriction modifier
16p partial trisomy syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Noonan syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of diaphragm Occurrence False Congenital Inferred relationship Existential restriction modifier
Sanfilippo syndrome Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Congenital anomaly of nervous system Occurrence False Congenital Inferred relationship Existential restriction modifier
Anomalous implantation of ureter Occurrence False Congenital Inferred relationship Existential restriction modifier
Anomalous muscle bands of right ventricle Occurrence False Congenital Inferred relationship Existential restriction modifier
Zellweger syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Lateral developmental cyst of jaw Occurrence False Congenital Inferred relationship Existential restriction modifier
Nagele's pelvis Occurrence False Congenital Inferred relationship Existential restriction modifier
Coronary artery arising from aorta Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of spermatic cord Occurrence False Congenital Inferred relationship Existential restriction modifier
Cheilognathoprosoposchisis Occurrence False Congenital Inferred relationship Existential restriction modifier
Kyphosis deformity of spine Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of cervix Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital hypoplastic anemia Occurrence False Congenital Inferred relationship Existential restriction modifier
Xeroderma pigmentosum, variant form Occurrence False Congenital Inferred relationship Existential restriction modifier
4q partial trisomy syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital hypoplasia of breast Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of liver Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital web of esophagus Occurrence False Congenital Inferred relationship Existential restriction modifier
Polymelia Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital prolapsed uterus Occurrence False Congenital Inferred relationship Existential restriction modifier
Crigler-Najjar syndrome, type I Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Anencephalus Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital displacement of stomach Occurrence False Congenital Inferred relationship Existential restriction modifier
Prader-Willi syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Gastrothoracopagus dipygus Occurrence False Congenital Inferred relationship Existential restriction modifier
Complete aphalangia of lower limb Occurrence False Congenital Inferred relationship Existential restriction modifier
Oromandibular-limb hypogenesis spectrum Occurrence False Congenital Inferred relationship Existential restriction modifier
Shwachman syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Persistent human tail Occurrence False Congenital Inferred relationship Existential restriction modifier
Tetrahydrofolate methyltransferase deficiency Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Glycogen storage disease, type VII Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Katadidymus Occurrence False Congenital Inferred relationship Existential restriction modifier
Pyknodysostosis Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital neutropenia Occurrence True Congenital Inferred relationship Existential restriction modifier 2
Congenital genu valgum Occurrence False Congenital Inferred relationship Existential restriction modifier
Transposition of colon Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of skeletal muscle Occurrence False Congenital Inferred relationship Existential restriction modifier
Ectopic pancreatic tissue in stomach Occurrence False Congenital Inferred relationship Existential restriction modifier
Abnormal umbilical cord Occurrence False Congenital Inferred relationship Existential restriction modifier
Collagen deficiency syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Hereditary orotic aciduria, type 2 Occurrence False Congenital Inferred relationship Existential restriction modifier
Fetus papyraceous Occurrence False Congenital Inferred relationship Existential restriction modifier
Frontal bossing Occurrence False Congenital Inferred relationship Existential restriction modifier
Porokeratosis of Mibelli, linear unilateral type Occurrence False Congenital Inferred relationship Existential restriction modifier
Autositic twin of asymmetrical conjoined twins Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital absence of aorta Occurrence False Congenital Inferred relationship Existential restriction modifier
Generalized epidermolysis bullosa simplex Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of artery Occurrence False Congenital Inferred relationship Existential restriction modifier
Carnitine palmitoyltransferase deficiency Occurrence True Congenital Inferred relationship Existential restriction modifier 1
Autosomal recessive hypophosphatemic vitamin D refractory rickets Occurrence False Congenital Inferred relationship Existential restriction modifier
Inflammatory disorder due to increased blood urate level Occurrence False Congenital Inferred relationship Existential restriction modifier
Persistent lanugo Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital diverticulum of stomach Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital asymmetry of jaw Occurrence False Congenital Inferred relationship Existential restriction modifier
3q partial trisomy syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Cordate pelvis Occurrence False Congenital Inferred relationship Existential restriction modifier
Unilateral congenital subluxation of hip Occurrence False Congenital Inferred relationship Existential restriction modifier
Muscle adenosine monophosphate deaminase deficiency Occurrence False Congenital Inferred relationship Existential restriction modifier
Warburg syndrome Occurrence False Congenital Inferred relationship Existential restriction modifier
Cephalodymus Occurrence False Congenital Inferred relationship Existential restriction modifier
Sirenomelia sequence Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anomaly of eyelid Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital anourethral fistula Occurrence False Congenital Inferred relationship Existential restriction modifier
Congenital rectourethral fistula Occurrence False Congenital Inferred relationship Existential restriction modifier
Disorder of the gamma-glutamyl cycle Occurrence False Congenital Inferred relationship Existential restriction modifier

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