Category:Genetic Disorders: Difference between revisions
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Latest revision as of 16:13, 3 February 2024
This is a category page. It lists all of the pages in category "Genetic Disorders" as well as all subcategories of category "Genetic Disorders" if any exist.
Pages in category "Genetic Disorders"
The following 200 pages are in this category, out of 810 total.
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- Aaas
- ABCD syndrome
- Abdallat Davis Farrage syndrome
- Abraham
- Abruzzo Erickson syndrome
- Acatalasia
- Acheiria
- Achondrogenesis
- Achondroplasia
- Acid lipase disease
- Acrocephalosyndactyly
- Acrocephaly
- Acrodysostosis
- Acrokeratosis verruciformis
- Acromicric dysplasia
- Activated protein C resistance
- Adactyly
- Adams Oliver syndrome
- Adducted thumb syndrome
- Adenylosuccinase deficiency
- Adermatoglyphia
- Adrenoleukodystrophy
- Adult polyglucosan body disease
- Afibrinogenemia
- Agammaglobulinemia
- Aicardi syndrome
- Al-Raqad syndrome
- Alba
- Albers
- Albino
- Alkaptonuria
- Alpers disease
- Alpers syndrome
- Alpha thalassemia
- Alpha-thalassemia
- Alport syndrome
- Amelogenesis imperfecta
- Amino acid disorder
- Amino acid transport disorder
- Aminoaciduria
- Aminolevulinic acid dehydratase deficiency porphyria
- Amish lethal microcephaly
- Analbuminaemia
- Andersen
- Andersen-Tawil syndrome
- Anderson
- Androgen insensitivity syndrome
- Androgen Insensitivity Syndrome
- Angelman Syndrome
- Anodontia
- Anophthalmia
- Apolipoprotein B deficiency
- Apulia
- Arachnodactyly
- Argininemia
- Armstrong
- Aromatase deficiency
- Aromatase excess syndrome
- Arrhythmogenic cardiomyopathy
- Arrhythmogenic right ventricular cardiomyopathy
- ARSA
- Arterial tortuosity syndrome
- Asfotase alfa
- Ataluren
- Ataxia telangiectasia
- Ataxia-pancytopenia syndrome
- Ataxia-telangiectasia
- ATR-X syndrome
- Atrichia with papular lesions
- Austin
- Autoimmune polyendocrine syndrome type 1
- Autoinflammatory syndrome
- Autoinflammatory syndromes
- Autosomal dominant disorder
B
- Baller-Gerold syndrome
- Bangstad syndrome
- Bardet-biedl syndrome
- Bare lymphocyte syndrome
- Bare lymphocyte syndrome 2
- Barth
- Barth syndrome
- Bartter's syndrome
- Batten disease
- Becker's muscular dystrophy
- Benign familial neonatal seizures
- Benjamin syndrome
- Berk-Tabatznik syndrome
- Bernadette Modell
- Beta ketothiolase deficiency
- Beta thalassemia
- Beta-ketothiolase deficiency
- Beta-thalassemia
- Bethlem myopathy
- Bhaskar Jagannathan syndrome
- Biemond syndrome
- Bietti's crystalline dystrophy
- Bifid nose
- Bifid uvula
- Birt-Hogg-Dube syndrome
- Bisalbuminemia
- Bleeder
- Bloch
- Blood coagulation disorders
- Bloom
- Blue cone monochromatism
- Bone deformity
- Boomerang dysplasia
- Brachydactyly
- Brachydactyly type A1
- Brachydactyly type C
- Brachydactyly type D
- Brachydactyly type E
- Brugada syndrome
- Brugada Syndrome
- Brunner syndrome
- Brushfield spots
- BSCL
- Burnside-Butler syndrome
C
- CADASIL
- Cadasil
- Camisa disease
- Camurati–Engelmann disease
- CAPS
- Carney syndrome
- Cartilage hair hypoplasia
- Caudal regression syndrome
- Cavernomas
- CD25 deficiency
- CD55 deficiency
- CDKL5 deficiency disorder
- Central hypoventilation syndrome
- Centrifugal lipodystrophy
- Centrofacial lentiginosis
- Centronuclear myopathy
- Cerebellar hypoplasia
- Cerebrotendineous xanthomatosis
- Channelopathy
- Char
- Char syndrome
- Charcot Marie Tooth disease
- Charcot-marie-tooth disease
- Charge syndrome
- Cherub
- CHILD syndrome
- Childhood tumor syndrome
- Chondrodysplasia
- Chondrodysplasia, Grebe type
- Chondrodystrophy
- Christianson syndrome
- Christmas disease
- Chromosomal disorders
- Chromosome instability syndrome
- Chronic granulomatous disease
- Chronic progressive external ophthalmoplegia
- Cleidocranial dysostosis
- Cleidocranial dysplasia
- Clinic for Special Children
- Clonal hypereosinophilia
- CLOVES syndrome
- Coenzyme Q10 deficiency
- Cohen syndrome
- Combined immunodeficiencies
- Complement deficiency
- Cone dystrophy
- Congenital adrenal hyperplasia
- Congenital afibrinogenemia
- Congenital cataract
- Congenital deafness
- Congenital disorder
- Congenital hepatic fibrosis
- Congenital hereditary endothelial dystrophy
- Congenital hyperinsulinism
- Congenital hypofibrinogenemia
- Congenital insensitivity to pain
- Congenital malformation
- Congenital muscular dystrophy
- Congenital myasthenic syndrome
- Congenital myopathy
- Congenital nephrotic syndrome
- Copenhagen disease
- Cornelia de Lange
- Cornelia de Lange syndrome
- Cornelia de lange syndrome
- Costeff syndrome
- Costello syndrome
- Craniodiaphyseal dysplasia
- Craniofacial abnormalities
- Craniofacial abnormality
- Craniofacial dysostosis
- Cree
- Crouzon Syndrome
- Cryptophthalmos
- Curacao
- Currarino syndrome
- Cutis laxa
- Cystathioninuria
- Cystic Fibrosis
- Cystinosis
- Cystinuria