Congenital heart disease ptosis hypodontia craniostosis

Congenital syphilis

Congenital dermal sinus

Congenital heart defect

Congenital melanocytic nevus

Congenital rubella syndrome

Congenital diaphragmatic hernia

Congenital cataract

Congenital anosmia

Congenital limb deformities

Congenital hypothyroidism

Congenital ichthyosiform erythroderma

Congenital insensitivity to pain

Congenital muscular dystrophy

Congenital amputation

Congenital myopathy

Congenital malaria

Congenital adrenal hyperplasia

Congenital dyserythropoietic anemia

Congenital absence of the vas deferens

Severe congenital neutropenia

Congenital chloride diarrhea

Congenital myasthenic syndrome

Congenital nephrotic syndrome

Leber congenital amaurosis

Congenital heart block

Congenital hemolytic anemia

Congenital hypoplastic anemia

Congenital lip pit

Late onset congenital adrenal hyperplasia

Congenital lactic acidosis

Congenital fiber type disproportion

Non-progressive congenital ataxia

Congenital pulmonary airway malformation

Congenital vertebral anomaly

Congenital dyserythropoietic anemia type IV

Congenital hypofibrinogenemia

Primary congenital glaucoma

Congenital generalized lipodystrophy

Congenital blindness

Congenital contractural arachnodactyly

Congenital iodine deficiency syndrome

List of ICD-9 codes 740–759: congenital anomalies

Congenital portosystemic shunt

Congenital stationary night blindness

Congenital onychodysplasia of the index fingers

Congenital fourth nerve palsy

Ullrich congenital muscular dystrophy

Congenital hereditary endothelial dystrophy

Fukuyama congenital muscular dystrophy

Congenital hyperinsulinism

Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome

Congenital stromal corneal dystrophy

Congenital distal spinal muscular atrophy

Congenital dyserythropoietic anemia type III

Congenital cartilaginous rest of the neck

Congenital dyserythropoietic anemia type I

Lethal congenital contracture syndrome

Distichiasis, congenital heart defects and mixed peripheral vascular anomalies

Congenital varicella syndrome

Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency

Congenital disorder of glycosylation

Congenital dyserythropoietic anemia type II

Congenital athymia

Isolated congenital asplenia

Congenital afibrinogenemia

Congenital clasped thumb

Congenital red–green color blindness

LMNA-related congenital muscular dystrophy

World Journal for Pediatric and Congenital Heart Surgery

Congenital hepatic fibrosis

Congenital erosive and vesicular dermatosis

List of congenital disorders

Congenital amegakaryocytic thrombocytopenia

Congenital pseudarthrosis of the tibia

Congenital smooth muscle hamartoma

Late congenital syphilitic oculopathy

Congenital stenosis of vena cava

Congenital Heart Surgeons' Society

Hypomyelination-congenital cataract syndrome

Congenital trigger thumb

Aplasia cutis congenita

Congenital cytomegalovirus infection

Compton-North congenital myopathy

Gunther disease

Congenital tufting enteropathy

LAMA2 related congenital muscular dystrophy

Absence of fingerprints-congenital milia syndrome

Congenital fibrosis of the extraocular muscles

Rocker bottom foot

Congenital epulis

Congenital disorder of glycosylation type IIc

Congenital mirror movement disorder

Fibular hemimelia

Amaurosis congenita, cone-rod type, with congenital hypertrichosis

Mesoblastic nephroma

Congenital insensitivity to pain with anhidrosis

Lipoid congenital adrenal hyperplasia

Multiple congenital anomalies-hypotonia-seizures syndrome

Cutis marmorata telangiectatica congenita

Multiple abnormalities

Hypertrichosis 1 (universalis, congenital)

Urinary tract obstruction

Congenital Agenesis of Gender Ideation

Congenital hearing loss

Congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase deficiency

Congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Congenital malformations of the dermatoglyphs

Nasolacrimal duct obstruction

Preauricular sinus and cyst

Congenital bilateral perisylvian syndrome

Congenital contractural arachnodactyly in cattle

Zonular cataract and nystagmus

X-linked hypertrichosis

Constriction ring syndrome

Congenital self-healing reticulohistiocytosis

Congenital adrenal hyperplasia due to 17α-hydroxylase deficiency

National Congenital Heart Disease Audit

Congenital cutaneous candidiasis

Central hypoventilation syndrome

Isolated hypogonadotropic hypogonadism

Sucrose intolerance

Alveolar capillary dysplasia

Kindler syndrome

Cataract-microcornea syndrome

Congenital sensorineural deafness in cats

Elimination Initiative

PMM2 deficiency

Congenital hypertrophy of the lateral fold of the hallux

Infantile esotropia

Congenital hypertrophy of the retinal pigment epithelium

Factor X deficiency

Proximal femoral focal deficiency

PELVIS syndrome

Worster-Drought syndrome

Posterior urethral valve

Primary lymphedema

Ichthyosis with confetti

Epidermolytic hyperkeratosis

Hypoplasminogenemia

Sonoda syndrome

Choledochal cysts

Multi/minicore myopathy

Spondyloepiphyseal dysplasia congenita

Multifocal lymphangioendotheliomatosis

Congenital disorders of amino acid metabolism

Centronuclear myopathy

Infantile hemangiopericytoma

Scimitar syndrome

Arteriovenous fistula

Adducted thumb syndrome

Umbilical hernia

Cardiocranial syndrome, Pfeiffer type

Microvillous inclusion disease

Inborn errors of metabolism

Stiff skin syndrome

Noonan syndrome

Bicuspid aortic valve

Levo-Transposition of the great arteries

Aromatase deficiency

Myotonic dystrophy

Klippel–Feil syndrome

Abdominal wall defect

Cervical spinal stenosis

Keratosis linearis with ichthyosis congenita and sclerosing keratoderma syndrome

Vaginal atresia

Isolated growth hormone deficiency

Neurotrophic keratitis

Caudal regression syndrome