Category:Genetic disorders
Revision as of 16:15, 3 February 2024 by Automatic category creator (talk | contribs) (Created automatically by the AutoCreateCategoryPages extension.)
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 638 total.
(previous page) (next page)1
2
3
A
- Aagenaes syndrome
- Aarskog Scott syndrome
- Aarskog syndrome
- Aase syndrome
- Abetalipoproteinemia
- Abiotrophy
- Ablepharon macrostomia syndrome
- ACDC
- Aceruloplasminemia
- Achalasia microcephaly
- Achard syndrome
- Acheiropodia
- Achondrogenesis type 2
- Achromatopsia
- Acid maltase deficiency
- Ackerman syndrome
- Acrocallosal syndrome
- Acrodermatitis enteropathica
- Acrofrontofacionasal dysostosis
- Acrogeria
- Acrokeratoelastoidosis of Costa
- Acromesomelic dysplasia
- Acropectoral syndrome
- Activated PI3K delta syndrome
- Acute intermittent porphyria
- Adenosine deaminase deficiency
- Advanced sleep phase disorder
- AFF2
- Alagille syndrome
- Albinism deafness syndrome
- Albinism in humans
- Albinism–deafness syndrome
- Alcaptonuria
- Alcohol flush reaction
- Aldolase A deficiency
- Aldred syndrome
- Alexander disease
- ALG1-CDG
- Alglucosidase alfa
- Alpha-L-iduronidase
- Alpha-mannosidosis
- Alternating
- Alternating hemiplegia
- Amelia (birth defect)
- Aminoacylase 1 deficiency
- Amyotrophic Lateral Sclerosis
- Angelman syndrome
- Ankyloblepharon
- Anonychia
- Anticipation (genetics)
- Antithrombin III deficiency
- Antithrombin iii deficiency
- Antley Bixler syndrome
- Apert syndrome
- AREDYLD syndrome
- Arginase deficiency
- Argininosuccinic acid
- Argininosuccinic aciduria
- Arts syndrome
- Aspartylglucosaminuria
- Atelosteogenesis, type II
- Atransferrinemia
- Atrophodermia vermiculata
- Avalglucosidase alfa
- Axenfeld-Rieger syndrome
B
- Barakat syndrome
- Barber Say syndrome
- Bardet-Biedl syndrome
- Bart syndrome
- Bartter syndrome
- Bart–Pumphrey syndrome
- Becker muscular dystrophy
- Beckwith-Wiedemann syndrome
- Behr syndrome
- Benign hereditary chorea
- BENTA disease
- Beta-mannosidosis
- Biotinidase deficiency
- Birk-Barel syndrome
- Bjornstad syndrome
- Blau syndrome
- Bloom syndrome
- Bohring-Opitz syndrome
- Bowen-Conradi syndrome
- Brachydactyly type A2
- Brachydactyly type A4
- Brachydactyly type B
- Branchio-oto-renal syndrome
- Branchiootorenal syndrome
- Brittle cornea syndrome
- Brody myopathy
- Bruck syndrome
- Bruton's tyrosine kinase
- Buschke Ollendorff syndrome
- Buschke–Ollendorff syndrome
C
- Cafe au lait spot
- Caffey disease
- CAMFAK syndrome
- Campomelic dysplasia
- Camptodactyly
- Canavan disease
- Carnitine palmitoyltransferase I
- Carnitine palmitoyltransferase I deficiency
- Carpenter syndrome
- Cartilage–hair hypoplasia
- Cask
- Cat eye syndrome
- Catel Manzke syndrome
- CDK13-related disorder
- CEDNIK syndrome
- Cenani Lenz syndactylism
- Central core disease
- Cernunnos deficiency
- Channelopathies
- Charcot-Marie-Tooth disease
- CHARGE syndrome
- Chediak-Higashi Syndrome
- Chediak-Higashi syndrome
- Cherubism
- CHIME syndrome
- Chondrodysplasia punctata
- Chondroectodermal dysplasia
- Chorea-acanthocytosis
- Choroideremia
- Chromosome 15q partial deletion
- Chromosome 15q trisomy
- Chromosome 2q deletion
- Chromosome 5q deletion syndrome
- Chromosome disorders
- Chylomicron retention disease
- Ciliopathy
- Citrullinemia
- Citrullinemia type I
- Citrullinemia type II
- Clouston's hidrotic ectodermal dysplasia
- COACH syndrome
- Coarse facial features
- Cockayne syndrome
- COL11A1
- Coloboma
- Complement 2 deficiency
- Complement 4 deficiency
- Congenital chloride diarrhea
- Congenital disorders of amino acid metabolism
- Congenital disorders of glycosylation
- Congenital hemolytic anemia
- Conorenal syndrome
- Cornea plana 1
- Cornea plana 2
- Corneal dystrophy
- Corneodermatoosseous syndrome
- Cortisone reductase deficiency
- Cowden syndrome
- Crandall syndrome
- Cranioectodermal dysplasia
- Craniofrontonasal dysplasia
- Cri du chat syndrome
- Cri du Chat Syndrome
- Crigler-Najjar syndrome
- Crome syndrome
- Cross syndrome
- Crouzon syndrome
- Crouzonodermoskeletal syndrome
- Cutis Verticis Gyrata
- Cytochrome b5 deficiency