Category:Congenital disorders
From WikiMD.com Medical Encyclopedia
 | This category reflects the organization of International Statistical Classification of Diseases and Related Health Problems, 10th Revision. Generally, diseases outlined within the ICD-10 codes Q00-Q99 should be included in this category. |
In medicine, a congenital disorder is a disorder that is present at birth.
Wikimedia Commons has media related to
.
Subcategories
This category has the following 10 subcategories, out of 10 total.
A
C
E
I
T
Pages in category "Congenital disorders"
The following 200 pages are in this category, out of 591 total.
(previous page) (next page)A
- A3P5PS
- Aagenaes syndrome
- Ablepharon macrostomia syndrome
- Absence deformity of leg-cataract syndrome
- Absent adrenal gland
- Absent body parts
- Acalvaria
- Acephaly
- Acheilia
- Acheiria
- Acheiropodia
- Achondrogenesis
- Acrania
- Acro-oto-radial syndrome
- Adams–Oliver syndrome
- Adducted thumb syndrome
- Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome
- Agenesis
- Agenesis of the vena cava
- Aglossia
- Agnathia
- Alveolar capillary dysplasia
- Amastia
- Amazia
- Amc
- Amelia
- Amelia (birth defect)
- Amorphous globosus
- Aneurysm of sinus of Valsalva
- Angioma serpiginosum
- Ankyloblepharon
- Anonychia-onychodystrophy with brachydactyly type B and ectrodactyly
- Anorectal anomalies
- Anotia
- Anterior segment mesenchymal dysgenesis
- Aphalangy-syndactyly-microcephaly syndrome
- Aposthia
- Aprosopus
- Aqueductal stenosis
- Intracranial cysts
- Armless
- Arrhinia
- Arteriovenous malformation
- Asplenia with cardiovascular anomalies
- Asymmetric crying facies
- Ateliosis
- Athelia
- Atransferrinemia
- Atresia
B
- Bamforth–Lazarus syndrome
- Bartsocas-Papas syndrome
- Bartter syndrome
- Bartter syndrome type 3
- Beckwith Wiedemann syndrome
- Bifid
- Biliary hypoplasia
- Birth defect
- Bladder exstrophy
- Bochdalek hernia
- Bone malrotation
- Bonnet Dechaume Blanc syndrome
- Bonnet–Dechaume–Blanc syndrome
- Boomerang dysplasia
- Bosma arhinia microphthalmia syndrome
- Brachydactyly
- Brachydactyly type D
- Brachymetatarsia
- Branchial cleft cyst
- Buphthalmos
C
- Camptodactyly joint contractures facial skeletal dysplasia
- Camptodactyly vertebral fusion
- Cantú syndrome
- Cardiocranial syndrome, Pfeiffer type
- Cardiofacial syndrome short limbs
- Cardiogenetic disorders
- Cardiomelic syndrome Stratton Koehler type
- Carey Fineman Ziter syndrome
- Carnevale–Krajewska–Fischetto syndrome
- Caroli disease
- Carpenter syndrome
- Cassia–Stocco–Dos Santos syndrome
- Cataract, congenital ichthyosis
- Caudal duplication
- Caudal regression sequence
- Cavernous hemangioma
- CDH
- CDK13-related disorder
- Cebocephaly
- CELSR1
- Central core disease
- Central nervous system cavernous hemangioma
- Cephalic disorder
- Cerebellar agenesis
- Cerebellar hypoplasia
- Cerebral calcification cerebellar hypoplasia
- Cerebral palsy
- Cervical agenesis
- Char syndrome
- CHD
- Chg
- Chiari malformation
- Chitayat–Meunier–Hodgkinson syndrome
- 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 lip palate incisor and finger anomalies
- Cleft palate incidence by population
- Cleft tongue syndrome
- CLOVES syndrome
- Club Foot
- Clubfoot
- Clutton's joints
- Cobb syndrome
- Colavita–Kozlowski syndrome
- Collaural fistula
- Colloid cyst
- Coloboma
- Colobomatous microphthalmia
- Colpocephaly
- Congenital
- Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
- Congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase deficiency
- Congenital amputation
- Congenital amputations
- Congenital anosmia
- Congenital articular rigidity
- Congenital athymia
- Congenital bilateral perisylvian syndrome
- Congenital brain disorder
- 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 hearing loss
- Congenital heart block
- Congenital heart disease ptosis hypodontia craniostosis
- 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
- Template:Congenital-stub
- Constriction ring syndrome
- Corpus callosum dysgenesis
- Cote–Katsantoni syndrome
- Coxa valga
- Craniofacial abnormality
- Craniofacial cleft
- Craniofrontonasal dysplasia
- Craniopagus parasiticus
- Craniorhiny
- Craniosynostosis
- Craniosynostosis mental retardation clefting syndrome
- Craniosynostosis, Adelaide type
- Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome
- Cri
- Crossed polydactyly type 1
- Cryptomicrotia brachydactyly syndrome
- Cryptophthalmos
- Currarino syndrome
- Cutis marmorata telangiectatica congenita
- Cyclopia
- Cystic hygroma
- Cytomegalic inclusion body disease
