Congenital Rubella Syndrome

Congenital dermal sinus

Congenital syphilis

Congenital heart defect

Congenital melanocytic nevus

Congenital rubella syndrome

Congenital cataract

Congenital hypothyroidism

Congenital diaphragmatic hernia

Congenital anosmia

Congenital insensitivity to pain

Congenital muscular dystrophy

Congenital limb deformities

Congenital amputation

Congenital myopathy

Congenital ichthyosiform erythroderma

Congenital malaria

Congenital adrenal hyperplasia

Congenital dyserythropoietic anemia

Congenital absence of the vas deferens

Severe congenital neutropenia

Congenital myasthenic syndrome

Leber congenital amaurosis

Congenital chloride diarrhea

Congenital heart block

Congenital nephrotic syndrome

Congenital hemolytic anemia

Congenital lip pit

Congenital hypoplastic anemia

Late onset congenital adrenal hyperplasia

Non-progressive congenital ataxia

Congenital vertebral anomaly

Congenital pulmonary airway malformation

Congenital fiber type disproportion

Congenital generalized lipodystrophy

Congenital hypofibrinogenemia

Congenital dyserythropoietic anemia type IV

Congenital blindness

Congenital lactic acidosis

Primary congenital glaucoma

Congenital iodine deficiency syndrome

Congenital contractural arachnodactyly

Congenital portosystemic shunt

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

Congenital stationary night blindness

Congenital fourth nerve palsy

Congenital hereditary endothelial dystrophy

Congenital onychodysplasia of the index fingers

Ullrich congenital muscular dystrophy

Congenital hyperinsulinism

Fukuyama congenital muscular dystrophy

Congenital distal spinal muscular atrophy

Congenital stromal corneal dystrophy

Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome

Congenital cartilaginous rest of the neck

Congenital dyserythropoietic anemia type III

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 disorder of glycosylation

Congenital varicella syndrome

Congenital athymia

Congenital dyserythropoietic anemia type II

Congenital afibrinogenemia

Congenital clasped thumb

Isolated congenital asplenia

Congenital red–green color blindness

LMNA-related congenital muscular dystrophy

World Journal for Pediatric and Congenital Heart Surgery

Congenital hepatic fibrosis

Congenital amegakaryocytic thrombocytopenia

List of congenital disorders

Congenital stenosis of vena cava

Late congenital syphilitic oculopathy

Congenital erosive and vesicular dermatosis

Congenital pseudarthrosis of the tibia

Congenital smooth muscle hamartoma

Congenital trigger thumb

Congenital Heart Surgeons' Society

Aplasia cutis congenita

Hypomyelination-congenital cataract syndrome

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 mirror movement disorder

Fibular hemimelia

Congenital disorder of glycosylation type IIc

Cutis marmorata telangiectatica congenita

Congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase deficiency

Lipoid congenital adrenal hyperplasia

Multiple congenital anomalies-hypotonia-seizures syndrome

Amaurosis congenita, cone-rod type, with congenital hypertrichosis

Congenital hearing loss

Urinary tract obstruction

Hypertrichosis 1 (universalis, congenital)

Congenital insensitivity to pain with anhidrosis

Mesoblastic nephroma

Multiple abnormalities

Congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Congenital Agenesis of Gender Ideation

Nasolacrimal duct obstruction

Congenital bilateral perisylvian syndrome

Constriction ring syndrome

Preauricular sinus and cyst

Congenital malformations of the dermatoglyphs

Congenital contractural arachnodactyly in cattle

Zonular cataract and nystagmus

Congenital adrenal hyperplasia due to 17α-hydroxylase deficiency

X-linked hypertrichosis

Central hypoventilation syndrome

Sucrose intolerance

Congenital self-healing reticulohistiocytosis

Congenital cutaneous candidiasis

Isolated hypogonadotropic hypogonadism

National Congenital Heart Disease Audit

Kindler syndrome

Alveolar capillary dysplasia

PMM2 deficiency

Cataract-microcornea syndrome

Elimination Initiative

Congenital sensorineural deafness in cats

Congenital hypertrophy of the retinal pigment epithelium

Congenital hypertrophy of the lateral fold of the hallux

Factor X deficiency

Proximal femoral focal deficiency

Infantile esotropia

Posterior urethral valve

Worster-Drought syndrome

Epidermolytic hyperkeratosis

PELVIS syndrome

Ichthyosis with confetti

Primary lymphedema

Hypoplasminogenemia

Multi/minicore myopathy

Choledochal cysts

Sonoda syndrome

Spondyloepiphyseal dysplasia congenita

Multifocal lymphangioendotheliomatosis

Centronuclear myopathy

Congenital disorders of amino acid metabolism

Infantile hemangiopericytoma

Scimitar syndrome

Arteriovenous fistula

Adducted thumb syndrome

Umbilical hernia

Cardiocranial syndrome, Pfeiffer type

Noonan syndrome

Microvillous inclusion disease

Inborn errors of metabolism

Stiff skin syndrome

Bicuspid aortic valve

Levo-Transposition of the great arteries

Aromatase deficiency

Myotonic dystrophy

Klippel–Feil syndrome

Abdominal wall defect

Cervical spinal stenosis

Vaginal atresia

Keratosis linearis with ichthyosis congenita and sclerosing keratoderma syndrome

Neurotrophic keratitis

Isolated growth hormone deficiency

Myasthenia gravis