Category:Congenital disorders
From WikiMD's Food, Medicine & Wellness 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.
Subcategories
This category has the following 7 subcategories, out of 7 total.
A
C
E
I
Pages in category "Congenital disorders"
The following 200 pages are in this category, out of 848 total.
(previous page) (next page)A
- Aagenaes syndrome
- Aarskog syndrome
- ABCC7
- Abdominal defects
- Abdominal wall defects
- Absence deformity of leg-cataract syndrome
- Absent body parts
- Acalvaria
- Acardiac twin
- Accessory auricle
- Accessory breast
- Accessory nipples
- Accessory pathway
- Accessory spleen
- Accessory talus
- Acheilia
- Achelia
- Achiria
- Achondrogenesis
- Acrania
- Acrodysostosis
- Adams–Nance syndrome
- Afibrinogenemia
- Agenesis
- Agenesis of corpus callosum
- Agenesis of the vena cava
- Aglossia
- Alcohol and pregnancy
- Amastia
- Amelia (birth defect)
- Amorphous globosus
- Ankyloglossia
- Anophthalmia megalocornea cardiopathy skeletal anomalies syndrome
- Anorectal anomalies
- Anorectal atresia
- Anotia
- Anterior segment mesenchymal dysgenesis
- Apical ectodermal ridge
- Aposthia
- Aprosencephaly cerebellar dysgenesis
- Aqueductal stenosis
- Arachnoid cysts
- Intracranial cysts
- Arakawa's syndrome II
- Arcuate uterus
- Armless
- Arteriovenous fistula
- Asphyxiating thoracic dysplasia 3
- Asplenia with cardiovascular anomalies
- Asymmetric crying facies
- Athelia
- Atransferrinemia
- Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome
B
- Bamforth–Lazarus syndrome
- Barakat syndrome
- Bartter syndrome
- Bartter syndrome type 3
- Basilar impression primary
- Benign congenital hypotonia
- Bifid nose dominant
- Bilateral optic nerve hypoplasia
- Biliary hamartomas
- Biliary hypoplasia
- Bladder exstrophy
- Blepharophimosis ptosis syndactyly mental retardation
- Blue baby
- Bochdalek hernia
- Bone deformity
- Bone dysplasia corpus callosum agenesis
- Bone malrotation
- Boomerang dysplasia
- Bowen-Conradi syndrome
- Brachycephaly deafness cataract mental retardation
- Brachydactyly clinodactyly
- Brachydactyly Smorgasbord type
- Brachydactyly type A3
- Brachydactyly type A5 nail dysplasia
- Brachydactyly type D
- Brachygnathism
- Brachymetatarsia
- Brachyturricephaly
- Branchial arch defects
- Branchial cleft
- Branchial cleft cyst
- Branchial fistula
- Breast aplasia
- Breast hypoplasia
- Brown syndrome
- Brown's
- Brugada syndrome
- Buphthalmos
C
- CAMFAK syndrome
- Camptodactyly
- Camptodactyly overgrowth unusual facies
- Camptodactyly vertebral fusion
- Cardiocranial syndrome, Pfeiffer type
- Cardiofacial syndrome short limbs
- Cardiomelic syndrome Stratton Koehler type
- Carey Fineman Ziter syndrome
- Caroli
- Cat eye syndrome
- Cataract, congenital ichthyosis
- Caudal duplication
- Caudal regression sequence
- CDH
- CDK13-related disorder
- Cebocephaly
- CELSR1
- Central core disease of muscle
- Central nervous system cavernous hemangioma
- Cephalopolysyndactyly
- Cerebral calcification cerebellar hypoplasia
- Cerebral palsy
- Cerebro facio thoracic dysplasia
- Cervical agenesis
- CFC1
- CHAOS
- Char syndrome
- CHD
- Chen-Kung Ho–Kaufman–Mcalister syndrome
- Choanal atresia
- Choledochal cyst
- Choledochal cyst, hand malformation
- Cholestasis pigmentary retinopathy cleft palate
- Chondrodysplasia situs inversus imperforate anus polydactyly
- Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature
- Circumscribed cutaneous aplasia of the vertex
- Cirsoid aneurysm
- Cleft Lip
- Cleft lip and cleft palate
- Cleft lip and palate
- Cleft lip palate abnormal thumbs microcephaly
- Cleft lip palate incisor and finger anomalies
- Cleft palate cardiac defect ectrodactyly
- Cleft palate colobomata radial synostosis deafness
- Cleft palate heart disease polydactyly absent tibia
- Cleft palate incidence by population
- Cleft palate X linked
- Cleft tongue syndrome
- Cleft uvula
- Cloacal septum
- Cloverleaf skull bone dysplasia
- Club Foot
- Clubbed thumb
- Clubfoot
- Clubhand
- Cmm
- Collaural fistula
- Coloboma
- Coloboma of iris
- Coloboma uveal with cleft lip palate and mental retardation
- Colobomata unilobar lung heart defect
- Colobomatous microphthalmia
- Compton-North congenital myopathy
- Congenital
- Congenital absence of the uterus and vagina
- Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
- Congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency
- Congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase deficiency
- Congenital amputation
- Congenital amputations
- Congenital anomalies
- Congenital anomaly
- Congenital arteriovenous shunt
- Congenital articular rigidity
- Congenital athymia
- Congenital bilateral perisylvian syndrome
- Congenital brain disorder
- Congenital bronchobiliary fistula
- Congenital cardiovascular disorder
- Congenital cardiovascular malformations
- Congenital cartilaginous rest of the neck
- Congenital cataract
- Congenital clasped thumb
- Congenital contractures
- Congenital craniosynostosis maternal hyperthyroiditis
- Congenital cystic adenomatoid malformation
- Congenital cytomegalovirus infection
- Congenital defect
- Congenital defects of phagocyte number, function, or both
- Congenital dermal sinus
- Congenital disorders of nervous system
- Congenital erosive and vesicular dermatosis
- Congenital fiber type disproportion
- Congenital fourth nerve palsy
- Congenital glaucoma
- Congenital heart disease ptosis hypodontia craniostosis
- Congenital hip dislocation
- Congenital hypertonia
- Congenital hypertrophy of the lateral fold of the hallux
