https://github.com/monarch-initiative/mondo/issues/4069

A characteristic of a disease in which the disease is present at birth, regardless of cause.

inborn

MONDO:0021140

• T-cell immunodeficiency, congenital alopecia, and nail dystrophy
• congenital hypotrichosis with juvenile macular dystrophy
• congenital cataract-hearing loss-severe developmental delay syndrome
• congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome
• pidermolysis bullosa, junctional 7, with interstitial lung disease and nephrotic syndrome
• cholesteatoma, congenital
• congenital tracheal stenosis
• Dyserythropoiesis, congenital, with ultrastructurally normal erythroblast heterochromatin
• congenital chylothorax
• congenital heart defects, multiple types, 3
• diabetes mellitus, congenital autoimmune
• congenital candidiasis
• myoclonic epilepsy, congenital deafness, macular dystrophy, and psychiatric disorders
• non-classic congenital adrenal hyperplasia
• facial palsy, congenital, with ptosis and velopharyngeal dysfunction
• nonsyndromic congenital nail disorder 7
• nonsyndromic congenital nail disorder 5
• congenital heart defects, multiple types, 5
• nonsyndromic congenital nail disorder 1
• muscular hypoplasia, congenital universal, of Krabbe
• cataract, congenital, with mental impairment and dentate gyrus atrophy
• cataract - congenital heart disease - neural tube defect syndrome
• aural atresia, congenital
• isolated congenital auditory ossicle malformation
• congenital nasal pyriform aperture stenosis with holoprosencephaly
• isolated congenital nasal pyriform aperture stenosis
• congenital epulis
• isolated congenital hypoglossia/aglossia
• congenital generalized lipodystrophy type 4
• congenital T-cell immunodeficiency
• multiple congenital anomalies-neurodevelopmental syndrome, X-linked
• congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency
• congenital bile acid synthesis defect 3
• nonsyndromic congenital nail disorder 9
• congenital enterovirus infection
• congenital varicella syndrome
• congenital rubella syndrome
• congenital microcoria
• congenital heart defects, multiple types, 7
• respiratory papillomatosis, juvenile recurrent, congenital
• congenital myopathy
• nonsyndromic congenital nail disorder 3
• congenital left-sided heart lesions
• glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form
• congenital bile acid synthesis defect 6
• congenital enteropathy involving intestinal mucosa development
• congenital intestinal transport defect
• quantitative and/or qualitative congenital phagocyte defect
• congenital pancreatic cyst
• congenital systemic veins anomaly
• congenital syphilis
• congenital disorder of glycosylation
• Bardet-Biedl syndrome
• congenital laryngeal cyst
• congenital subglottic stenosis
• congenital panfollicular nevus
• congenital radioulnar synostosis
• non-classic congenital lipoid adrenal hyperplasia due to STAR deficency
• classic congenital lipoid adrenal hyperplasia due to STAR deficency
• isolated congenital syngnathia
• nonsyndromic congenital nail disorder 6
• thumbs, congenital Clasped
• congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization
• congenital limb malformation
• adrenocortical hypofunction, chronic primary congenital
• multiple congenital anomalies/dysmorphic syndrome
• craniostenosis with congenital heart disease intellectual disability
• congenital vagal hyperreflexivity
• coronary arteries congenital malformation
• polycystic kidney, cataract, and congenital blindness
• congenital mumps
• congenital hypotrichosis milia
• congenital unilateral pulmonary hypoplasia
• congenital nonhemolytic jaundice
• congenital benign spinal muscular atrophy dominant
• lethal congenital glycogen storage disease of heart
• congenital aneurysms of the great vessels
• congenital amputation
• congenital absence of the sternocleidomastoid muscle
• congenital arteriovenous shunt
• congenital heart disease radio ulnar synostosis intellectual disability
• congenital heart disease ptosis hypodontia craniostosis
• congenital cystic eye
• pancreatic hypoplasia-diabetes-congenital heart disease syndrome
• congenital osteogenesis imperfecta-microcephaly-cataracts syndrome
• congenital alacrima
• congenital ectropion
• congenital entropion
• congenital glaucoma
• congenital symblepharon
• congenital heart defects and ectodermal dysplasia
• distichiasis heart congenital anomalies
• congenital pseudoarthrosis of clavicle
• hereditary hyperferritinemia with congenital cataracts
• congenital pulmonary lymphangiectasia
• congenital tricuspid malformation
• congenital pulmonary veins anomaly
• congenital arteriovenous fistula
• congenital anomaly of the great arteries