Category:Congenital disorders
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In medicine, a congenital disorder is a disorder that is present at birth.
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Subcategories
This category has the following 10 subcategories, out of 10 total.
Pages in category "Congenital disorders"
The following 200 pages are in this category, out of 494 total.
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- A3P5PS
- Aagenaes syndrome
- Ablepharon macrostomia syndrome
- Absence deformity of leg-cataract syndrome
- Absent adrenal gland
- Acalvaria
- Acephaly
- Acheilia
- Acheiropodia
- Achondrogenesis
- Acrania
- Adams–Oliver syndrome
- Adducted thumb syndrome
- Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome
- Agenesis
- Agenesis of the vena cava
- Aglossia
- Agnathia
- Amastia
- Amelia
- Amelia (birth defect)
- Amorphous globosus
- Aneurysm of sinus of Valsalva
- Angioma serpiginosum
- Ankyloblepharon
- Anorectal anomalies
- Anotia
- Anterior segment mesenchymal dysgenesis
- Aposthia
- Aqueductal stenosis
- Intracranial cysts
- Arrhinia
- Arteriovenous malformation
- Asplenia with cardiovascular anomalies
- Asymmetric crying facies
- Ateliosis
- Athelia
- Atransferrinemia
- Atresia
B
- Bamforth–Lazarus syndrome
- Bartter syndrome
- Bartter syndrome type 3
- Beckwith Wiedemann syndrome
- Bifid
- Birth defect
- Bladder exstrophy
- Bochdalek hernia
- Bone malrotation
- Bonnet–Dechaume–Blanc syndrome
- Boomerang dysplasia
- Bosma arhinia microphthalmia syndrome
- Brachydactyly
- Brachydactyly type D
- Brachydactyly-preaxial hallux varus syndrome
- Brachymetatarsia
- Branchial cleft cyst
- Buphthalmos
C
- Camptodactyly joint contractures facial skeletal dysplasia
- Cantú syndrome
- Cardiocranial syndrome, Pfeiffer type
- Cardiogenetic disorders
- Cardiomelic syndrome Stratton Koehler type
- Carey Fineman Ziter syndrome
- Carnevale–Krajewska–Fischetto syndrome
- Caroli disease
- Carpenter syndrome
- Caudal duplication
- Caudal regression sequence
- Cavernous hemangioma
- CDK13-related disorder
- Cebocephaly
- Central core disease
- Central nervous system cavernous hemangioma
- Cephalic disorder
- Cerebellar agenesis
- Cerebellar hypoplasia
- Cerebral calcification cerebellar hypoplasia
- Cerebral palsy
- Cervical agenesis
- Char syndrome
- Chiari malformation
- Choanal atresia
- Choledochal cyst
- Christian–Johnson–Angenieta syndrome
- Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature
- Cirsoid aneurysm
- Cleft lip and cleft palate
- Cleft palate incidence by population
- CLOVES syndrome
- Club Foot
- Clubfoot
- Coarse facial features
- Cobb syndrome
- Colloid cyst
- Coloboma
- Colpocephaly
- Congenital
- Congenital adrenal hyperplasia due to 17α-hydroxylase deficiency
- Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
- Congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase deficiency
- Congenital amputation
- Congenital anosmia
- Congenital athymia
- Congenital bilateral perisylvian syndrome
- Congenital cartilaginous rest of the neck
- Congenital cataract
- Congenital clasped thumb
- Congenital cytomegalovirus infection
- Congenital dermal sinus
- Congenital disorder of glycosylation type IIc
- Congenital disorders of nervous system
- Congenital erosive and vesicular dermatosis
- Congenital fiber type disproportion
- Congenital fourth nerve palsy
- Congenital heart block
- Congenital hepatic fibrosis
- Congenital hypertrophy of the lateral fold of the hallux
- Congenital hypothyroidism
- Congenital intrauterine infection-like syndrome
- Congenital iodine deficiency syndrome
- Congenital lactic acidosis
- Congenital limb deficiency
- Congenital limb deformities
- Congenital lip pit
- Congenital malformations of the dermatoglyphs
- Congenital myasthenic syndrome
- Congenital nephrotic syndrome Finnish type
- Congenital portosystemic shunt
- Congenital pulmonary airway malformation
- Congenital radioulnar synostosis
- Congenital rubella syndrome
- Congenital smooth muscle hamartoma
- Congenital stenosis of vena cava
- Congenital varicella syndrome
- Constriction ring syndrome
- Corpus callosum dysgenesis
- Cote–Katsantoni syndrome
- Coxa valga
- Craniofacial abnormality
- Craniofacial cleft
- Craniofrontonasal dysplasia
- Craniopagus parasiticus
- Craniosynostosis
- Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome
- Crossed polydactyly type 1
- Cryptophthalmos
- Currarino syndrome
- Cutis marmorata telangiectatica congenita
- Cyclopia
- Cystic hygroma
- Cytomegalic inclusion body disease
D
- D-glycerate dehydrogenase deficiency
- Daentl Townsend Siegel syndrome
- Dandy–Walker malformation postaxial polydactyly
- DDOST-CDG (CDG-Ir)
- Dennis–Fairhurst–Moore syndrome
- Diabetic embryopathy
- Diaphragmatic hernia
- Diaphragmatic hernia upper limb defects
- Diastematomyelia
- Dimitri–Sturge–Weber syndrome
- Distichiasis, congenital heart defects and mixed peripheral vascular anomalies
- Diverticulum
- Dolichocolon
- Donnai–Barrow syndrome
- Drachtman–Weinblatt–Sitarz syndrome
- Du Bois sign
- Du Pan syndrome
- Duane-radial ray syndrome
- Duplicated ureter
- Dysgenesis
- Dysmorphic feature
- Dysostosis
- Dysphagia lusoria
E
- Eclabium
- Ectrodactyly
- Ectrodactyly–ectodermal dysplasia–cleft syndrome
- Ectromelia
- Arthrochalasia Ehlers-Danlos syndrome
- Classical Ehlers-Danlos syndrome
- Dermatosparaxis Ehlers-Danlos syndrome
- Kyphoscoliotic Ehlers-Danlos syndrome
- Spondylodysplastic Ehlers-Danlos syndrome
- Ellis–Van Creveld syndrome
- Enteric duplication cyst
- Epidermal nevus syndrome
- Epignathus
- Epispadias
- Equinovalgus
- Esophageal inlet patch
