congenital
A characteristic of a disease in which the disease is present at birth, regardless of cause.
Exact Synonyms
inborn
class Information
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icd11.foundation:1048408993
term tracker item
class Relations
Subclass of
Related from
has characteristic
- familial adrenal hypoplasia with absent pituitary luteinizing hormone
- congenital hypotonia, epilepsy, developmental delay, and digital anomalies
- congenital heart defects, multiple types, 2
- brachial palsy, familial congenital
- congenital tracheal stenosis
- isolated congenital megalocornea
- familial progressive retinal dystrophy-iris coloboma-congenital cataract syndrome
- congenital panfollicular nevus
- congenital knee dislocation
- congenital heart defects, multiple types, 7
- familial isolated congenital asplenia
- skin creases, congenital symmetric circumferential, 2
- congenital reticular ichthyosiform erythroderma
- congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency
- congenital absence of both forearm and hand
- thyroid ectopia
- non-classic congenital adrenal hyperplasia
- congenital vascular malformation
- congenital pulmonary lymphangiectasia
- congenital radioulnar synostosis
- nonsyndromic congenital nail disorder 1
- congenital varicella syndrome
- congenital nonhemolytic jaundice
- channelopathy-associated congenital insensitivity to pain, autosomal recessive
- isolated congenital hypogonadotropic hypogonadism
- resistance to thyroid hormone due to a mutation in thyroid hormone receptor alpha
- congenital diarrhea
- congenital hemangioma
- congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency
- congenital anomaly of hepatic vein
- congenital heart defects, multiple types, 3
- hamartoma, Precalcaneal congenital fibrolipomatous
- Huppke-Brendel syndrome
- pancreatic hypoplasia-diabetes-congenital heart disease syndrome
- congenital agenesis of the scrotum
- large congenital melanocytic nevus
- congenital absence of upper arm and forearm with hand present
- diaphragmatic hernia 1
- congenital aneurysms of the great vessels
- congenital microcoria
- Friedreich ataxia and congenital glaucoma
- classic congenital lipoid adrenal hyperplasia due to STAR deficency
- congenital ichthyosis-microcephalus-tetraplegia syndrome
- congenital laryngeal cyst
- congenital rubella syndrome
- congenital shoulder dislocation
- congenital pseudoarthrosis of the limbs
- congenital mumps
- diabetes mellitus, congenital autoimmune
- congenital mesoblastic nephroma
- congenital/infantile spindle cell rhabdomyosarcoma with VGLL2/NCOA2/CITED2 rearrangements
- congenital generalized lipodystrophy type 4
- obesity due to leptin receptor gene deficiency
- Berardinelli-Seip congenital lipodystrophy
- muscular hypoplasia, congenital universal, of Krabbe
- congenital enteropathy due to enteropeptidase deficiency
- congenital absence of thigh and lower leg with foot present
- visceral steatosis, congenital
- congenital absence of both lower leg and foot
- isolated congenital hypoglossia/aglossia
- arthrogryposis, congenital, lower limb, X-linked
- nonsyndromic congenital nail disorder 7
- congenital aortic valve stenosis
- glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form
- congenital microgastria
- obesity due to congenital leptin deficiency
- congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization
- absence of fingerprints-congenital milia syndrome
- congenital subglottic stenosis
- congenital fibrosarcoma
- hypotonia, congenital nystagmus, ataxia, and abnormal auditory brainstem responses
- craniostenosis with congenital heart disease intellectual disability
- facial paresis, hereditary congenital, 3
- congenital amputation
- congenital syphilis
- congenital bile acid synthesis defect 3
- congenital sucrase-isomaltase deficiency
- familial thyroglossal duct cyst
- congenital disorder of glycosylation, type i/IIx
- thumbs, congenital Clasped
- congenital pulmonary airway malformation
- congenital bilateral absence of vas deferens
- congenital heart block
- congenital symblepharon
- congenital nasal pyriform aperture stenosis with holoprosencephaly
- congenital enterocyte heparan sulfate deficiency
- isolated congenitally uncorrected transposition of the great arteries
- congenital heart disease radio ulnar synostosis intellectual disability
- congenital short bowel syndrome, autosomal recessive
- congenital lactase deficiency
- adrenocortical hypofunction, chronic primary congenital
- congenital aortic valve insufficiency
- isolated congenital syngnathia
- respiratory papillomatosis, juvenile recurrent, congenital
- congenital vagal hyperreflexivity
- facial palsy, congenital, with ptosis and velopharyngeal dysfunction
- congenital myopathy
- congenital pseudoarthrosis of clavicle
- T-cell immunodeficiency, congenital alopecia, and nail dystrophy
- thyroid hypoplasia
- deafness, congenital, with total albinism
- congenital unilateral pulmonary hypoplasia
- isolated congenital nasal pyriform aperture stenosis
- nonsyndromic congenital nail disorder 3
- cranial nerves, congenital paresis of
- preauricular fistulae, congenital
- deafness, congenital, and familial myoclonic epilepsy
- congenital primary megaureter, obstructed form
- congenital deformities of limbs
- congenital elbow dislocation
- athyreosis
- non-classic congenital lipoid adrenal hyperplasia due to STAR deficency
- Ehlers-Danlos syndrome, spondylodysplastic type
- congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
- congenital bile acid synthesis defect 6
- congenital anomaly of the inferior vena cava
- congenital cystic eye
- congenital temporomandibular joint ankylosis
- congenital hypotrichosis with juvenile macular dystrophy
- multiple congenital anomalies-neurodevelopmental syndrome, X-linked
- polycystic kidney, cataract, and congenital blindness
- congenital megacalycosis
- congenital complete agenesis of pericardium
- distichiasis heart congenital anomalies
- nonsyndromic congenital nail disorder 5
- congenital ectropion
- cholesteatoma, congenital
- congenital heart defects, multiple types, 5
- lethal congenital glycogen storage disease of heart
- congenital arteriovenous fistula
- congenital left-sided heart lesions
- neonatal diabetes mellitus with congenital hypothyroidism
- adactylia, unilateral
- nonsyndromic congenital nail disorder 2
- congenital glaucoma
- congenitally uncorrected transposition of the great arteries with cardiac malformation
- congenital hematological disorder
- classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency
- autosomal recessive congenital ichthyosis
- Dyserythropoiesis, congenital, with ultrastructurally normal erythroblast heterochromatin
- congenital portosystemic shunt
- autosomal recessive nonsyndromic congenital nuclear cataract
- congenital disorder of glycosylation
- congenital brain dysgenesis due to glutamine synthetase deficiency
- congenital heart disease ptosis hypodontia craniostosis
- congenital cataract-severe neonatal hepatopathy-global developmental delay syndrome
- cataract - congenital heart disease - neural tube defect syndrome
- nonsyndromic congenital nail disorder 6
- linear skin defects with multiple congenital anomalies 1
- congenital nervous system disorder
- congenital heart defects, multiple types, 4
- congenital enterovirus infection
- linear skin defects with multiple congenital anomalies 3
- X-linked congenital generalized hypertrichosis
- isolated congenital auditory ossicle malformation
- congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency
- congenital stromal corneal dystrophy
- microcephaly-congenital cataract-psoriasiform dermatitis syndrome
- congenital osteogenesis imperfecta-microcephaly-cataracts syndrome
- congenitally uncorrected transposition of the great arteries with coarctation
- congenital patella dislocation, bilateral
- hydrocephalus, congenital communicating, 1
- Zika virus congenital syndrome
- congenital patella dislocation, unilateral
- thyroid hemiagenesis
- neonatal diabetes, congenital sensorineural hearing loss and congenital cataracts
- congenital bile acid synthesis defect 2
- epidermolysis bullosa, junctional 7, with interstitial lung disease and nephrotic syndrome
- congenital bile acid synthesis defect 4
- congenital erosive and vesicular dermatosis
- congenital pancreatic cyst
- tibia, absence of, with congenital deafness
- congenital Gerbode defect
- congenital aortopulmonary window
- congenital entropion
- hereditary hyperferritinemia with congenital cataracts
- NKX2.5-related congenital, conduction and myopathic heart disease
- Bardet-Biedl syndrome
- aural atresia, congenital
- congenital T-cell immunodeficiency
- facial paresis, hereditary congenital, 2
- congenital corneal opacities, cornea guttata, and corectopia
- congenital primary megaureter, refluxing form
- congenital coronary artery anomaly
- congenital contractures of the limbs and face, hypotonia, and developmental delay
- congenital tricuspid malformation
- congenital anomaly of the great arteries
- myoclonic epilepsy, congenital deafness, macular dystrophy, and psychiatric disorders
- congenital pulmonary veins anomaly
- congenital absence of the sternocleidomastoid muscle
- congenital chylothorax
- congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome
- congenital heart defects and ectodermal dysplasia
- congenital hypothyroidism
- congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency
- isolated congenital alacrima
- familial congenital nasolacrimal duct obstruction
- non-congenital cyst of kidney
- multiple congenital anomalies/dysmorphic syndrome
- cone-rod synaptic disorder syndrome, congenital nonprogressive
- congenital laryngeal web
- nonsyndromic congenital nail disorder 9
- congenital benign spinal muscular atrophy dominant
- congenital hypotrichosis milia
- epidermolysis bullosa with congenital localized absence of skin and deformity of nails
- congenital ectropion uveae
- obesity due to prohormone convertase I deficiency
- cataract, congenital, with mental impairment and dentate gyrus atrophy
- keratoconus and congenital hip dysplasia
- congenital smooth muscle hamartoma
- congenital candidiasis
- congenital mitral malformation
- congenital limb malformation
- lower urinary tract obstruction, congenital
- congenital hydronephrosis
- distichiasis with congenital anomalies of the heart and peripheral vasculature
- congenital esophageal diverticulum
- hypopituitarism, congenital, with central diabetes insipidus
- congenital partial agenesis of pericardium
- familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome