Congenital laryngomalacia

Congenital dermal sinus

Congenital syphilis

Congenital heart defect

Congenital melanocytic nevus

Congenital rubella syndrome

Congenital cataract

Congenital diaphragmatic hernia

Congenital hypothyroidism

Congenital anosmia

Congenital insensitivity to pain

Congenital muscular dystrophy

Congenital limb deformities

Congenital myopathy

Congenital amputation

Congenital ichthyosiform erythroderma

Congenital malaria

Congenital adrenal hyperplasia

Congenital dyserythropoietic anemia

Congenital absence of the vas deferens

Severe congenital neutropenia

Congenital chloride diarrhea

Congenital myasthenic syndrome

Leber congenital amaurosis

Congenital nephrotic syndrome

Congenital heart block

Congenital hypoplastic anemia

Congenital hemolytic anemia

Congenital lip pit

Non-progressive congenital ataxia

Late onset congenital adrenal hyperplasia

Congenital fiber type disproportion

Congenital pulmonary airway malformation

Congenital vertebral anomaly

Congenital generalized lipodystrophy

Congenital lactic acidosis

Congenital hypofibrinogenemia

Primary congenital glaucoma

Congenital blindness

Congenital dyserythropoietic anemia type IV

Congenital iodine deficiency syndrome

Congenital contractural arachnodactyly

Congenital stationary night blindness

Congenital portosystemic shunt

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

Congenital onychodysplasia of the index fingers

Ullrich congenital muscular dystrophy

Congenital hereditary endothelial dystrophy

Congenital fourth nerve palsy

Congenital distal spinal muscular atrophy

Fukuyama congenital muscular dystrophy

Congenital hyperinsulinism

Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome

Congenital stromal corneal dystrophy

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 adrenal hyperplasia due to 11β-hydroxylase deficiency

Congenital varicella syndrome

Congenital dyserythropoietic anemia type II

Congenital disorder of glycosylation

Congenital athymia

Congenital red–green color blindness

Isolated congenital asplenia

Congenital clasped thumb

Congenital afibrinogenemia

LMNA-related congenital muscular dystrophy

World Journal for Pediatric and Congenital Heart Surgery

Congenital hepatic fibrosis

Congenital amegakaryocytic thrombocytopenia

Congenital erosive and vesicular dermatosis

List of congenital disorders

Congenital pseudarthrosis of the tibia

Congenital smooth muscle hamartoma

Late congenital syphilitic oculopathy

Congenital stenosis of vena cava

Congenital Heart Surgeons' Society

Congenital trigger thumb

Hypomyelination-congenital cataract syndrome

Aplasia cutis congenita

Congenital cytomegalovirus infection

Compton-North congenital myopathy

Congenital tufting enteropathy

Gunther disease

LAMA2 related congenital muscular dystrophy

Congenital fibrosis of the extraocular muscles

Congenital epulis

Absence of fingerprints-congenital milia syndrome

Rocker bottom foot

Congenital disorder of glycosylation type IIc

Congenital mirror movement disorder

Fibular hemimelia

Lipoid congenital adrenal hyperplasia

Cutis marmorata telangiectatica congenita

Multiple congenital anomalies-hypotonia-seizures syndrome

Mesoblastic nephroma

Urinary tract obstruction

Amaurosis congenita, cone-rod type, with congenital hypertrichosis

Congenital insensitivity to pain with anhidrosis

Congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase deficiency

Hypertrichosis 1 (universalis, congenital)

Congenital hearing loss

Multiple abnormalities

Congenital Agenesis of Gender Ideation

Congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Nasolacrimal duct obstruction

Congenital malformations of the dermatoglyphs

Congenital bilateral perisylvian syndrome

Preauricular sinus and cyst

Constriction ring syndrome

Zonular cataract and nystagmus

Congenital contractural arachnodactyly in cattle

Congenital adrenal hyperplasia due to 17α-hydroxylase deficiency

X-linked hypertrichosis

Central hypoventilation syndrome

Congenital self-healing reticulohistiocytosis

National Congenital Heart Disease Audit

Sucrose intolerance

Congenital cutaneous candidiasis

Isolated hypogonadotropic hypogonadism

Kindler syndrome

Alveolar capillary dysplasia

Cataract-microcornea syndrome

PMM2 deficiency

Congenital sensorineural deafness in cats

Elimination Initiative

Congenital hypertrophy of the retinal pigment epithelium

Congenital hypertrophy of the lateral fold of the hallux

Infantile esotropia

Proximal femoral focal deficiency

Factor X deficiency

Posterior urethral valve

Worster-Drought syndrome

PELVIS syndrome

Epidermolytic hyperkeratosis

Primary lymphedema

Hypoplasminogenemia

Ichthyosis with confetti

Sonoda syndrome

Multi/minicore myopathy

Spondyloepiphyseal dysplasia congenita

Choledochal cysts

Multifocal lymphangioendotheliomatosis

Congenital disorders of amino acid metabolism

Centronuclear myopathy

Scimitar syndrome

Infantile hemangiopericytoma

Arteriovenous fistula

Adducted thumb syndrome

Umbilical hernia

Cardiocranial syndrome, Pfeiffer type

Microvillous inclusion disease

Noonan syndrome

Inborn errors of metabolism

Stiff skin syndrome

Bicuspid aortic valve

Levo-Transposition of the great arteries

Aromatase deficiency

Klippel–Feil syndrome

Myotonic dystrophy

Abdominal wall defect

Keratosis linearis with ichthyosis congenita and sclerosing keratoderma syndrome

Cervical spinal stenosis

Vaginal atresia

Isolated growth hormone deficiency

Neurotrophic keratitis

Infantile myofibromatosis