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.
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 867 total.
(previous page) (next page)A
- A3P5PS
- Aagenaes syndrome
- ABCC7
- Abdominal wall defects
- Ablepharon
- Ablepharon macrostomia syndrome
- Abnormity
- Absence deformity of leg-cataract syndrome
- Absent adrenal gland
- Absent body parts
- Acalvaria
- Acardiac twin
- Acephaly
- Acheilia
- Acheiria
- Acheiropodia
- Achondrogenesis
- Acrania
- Acrodysostosis
- Adducted thumb syndrome
- Afibrinogenemia
- Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome
- Aganglionic megacolon
- Aganglionosis, total intestinal
- Agenesis
- Agenesis of corpus callosum
- Agenesis of the vena cava
- Aglossia
- Agnathia
- Al Awadi Teebi Farag syndrome
- Alcohol and pregnancy
- Amastia
- Amazia
- Amc
- Amelia
- Amelia (birth defect)
- Amorphous globosus
- Anencephalus
- Ankyloblepharon
- Ankyloblepharon filiforme adnatum
- Anorectal anomalies
- Anotia
- Anterior segment mesenchymal dysgenesis
- Aorta-pulmonary artery fistula
- Aplasia cutis
- Aposthia
- Aprosencephaly-atelencephaly syndrome
- Aprosopus
- Aqueductal stenosis
- Intracranial cysts
- Armless
- Arnold Chiari malformation
- Arnold-Chiari malformations
- Arteriovenous fistula
- Arteriovenous malformation
- Arthrogryposis multiplex congenita, distal type 1
- Articulation of head of rib
- Asphyxiating thoracic dysplasia 3
- Asplenia with cardiovascular anomalies
- Asymmetric crying facies
- Ateliosis
- Athelia
- Atransferrinemia
- Atresia
- Atretic
- Autopodium
B
- Bamforth-Lazarus syndrome
- Bamforth–Lazarus syndrome
- Barakat syndrome
- Bartter syndrome
- Bartter syndrome type 3
- Bd syndrome
- Beckwith Wiedemann syndrome
- Beckwith-wiedemann syndrome
- Benign congenital hypotonia
- Bidactyly
- Bifid
- Bilateral optic nerve hypoplasia
- Biliary hypoplasia
- Bladder exstrophy
- Blepharoptosis
- Blue baby
- Bochdalek hernia
- Body stalk anomaly
- Bone deformity
- Bone malrotation
- Bonnet Dechaume Blanc syndrome
- Boomerang dysplasia
- Borrone Di Rocco Crovato syndrome
- Bosma arhinia microphthalmia syndrome
- Boudhina Yedes Khiari syndrome
- Bowen-Conradi syndrome
- Brachydactyly
- Brachydactyly Ballard type
- Brachydactyly Haws type
- Brachydactyly Smorgasbord type
- Brachydactyly type A3
- Brachydactyly type A5
- Brachydactyly type A5 nail dysplasia
- Brachydactyly type A7
- Brachydactyly type D
- Brachymetatarsia
- Branchial arch defects
- Branchial cleft
- Branchial cleft cyst
- Branchial fistula
- Breast aplasia
- Breast hypoplasia
- Brown syndrome
- Brown's
- Buphthalmos
C
- Cacchi Ricci disease
- Camptodactyly
- Camptodactyly joint contractures facial skeletal dysplasia
- Camptodactyly vertebral fusion
- Cantrell deformity
- Cantrell syndrome
- Cantú syndrome
- Cardiac valvular dysplasia, X-linked
- Cardiocranial syndrome, Pfeiffer type
- Cardiofacial syndrome short limbs
- Cardiogenetic disorders
- Cardiomelic syndrome Stratton Koehler type
- Carey Fineman Ziter syndrome
- Carnevale–Krajewska–Fischetto syndrome
- Cassia–Stocco–Dos Santos syndrome
- Cat eye syndrome
- Cataract, congenital ichthyosis
- Caudal duplication
- Caudal regression sequence
- Cayler cardiofacial syndrome
- CDH
- CDK13-related disorder
- Cebocephaly
- CELSR1
- Central core disease of muscle
- Central nervous system cavernous hemangioma
- Cephalopolysyndactyly
- Cerebellar hypoplasia
- Cerebral calcification cerebellar hypoplasia
- Cerebral palsy
- Cerebro reno digital syndrome
- Cervical agenesis
- CFC1
- Char syndrome
- Charge syndrome
- CHD
- Chen-Kung Ho–Kaufman–Mcalister syndrome
- Chg
- Chiari malformation
- Chiari type 1 malformation
- Chitayat–Meunier–Hodgkinson syndrome
- Choanal atresia
- Choledochal cyst
- Christian–Johnson–Angenieta syndrome
- Chromosome 18, trisomy
- Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature
- Cirsoid aneurysm
- Cleft lip
- Cleft Lip
- Cleft lip and cleft palate
- Cleft lip and palate
- Cleft lip palate incisor and finger anomalies
- Cleft lip with or without cleft palate
- Cleft palate
- Cleft Palate
- Cleft palate incidence by population
- Cleft palate X linked
- Cleft tongue syndrome
- Cleft uvula
- Clefted
- Cloverleaf skull bone dysplasia
- CLOVES syndrome
- Club feet
- Club Foot
- Clubfoot
- Clubhand
- Clutton's joints
- Coffin Siris syndrome
- Cohen-Gibson syndrome
- Colavita–Kozlowski syndrome
- Collaural fistula
- Coloboma
- Coloboma of iris
- Colobomata unilobar lung heart defect
- Colobomatous microphthalmia
- Congenital
- Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency
- Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
- Congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency
