A–Z DIRECTORY
Conditions beginning with A
- Aarskog-Scott syndromeAutosomal dominant · X-linked recessive · Autosomal recessive
- Abdominal wall defectPattern unknown
- AbetalipoproteinemiaAutosomal recessive
- ACAD9 deficiencyAutosomal recessive
- AcatalasemiaAutosomal recessive
- AceruloplasminemiaAutosomal recessive
- AchondrogenesisAutosomal recessive · Autosomal dominant, or a new variant
- AchondroplasiaAutosomal dominant
- AchromatopsiaAutosomal recessive
- Acrocallosal syndromeAutosomal recessive · Autosomal dominant
- Acromicric dysplasiaAutosomal dominant
- Actin-accumulation myopathyAutosomal dominant · Not inherited
- Action myoclonus–renal failure syndromeAutosomal recessive
- Activated PI3K-delta syndromeAutosomal dominant
- Acute necrotizing encephalopathy type 1Autosomal dominant
- Acute promyelocytic leukemiaNot inherited
- Adams-Oliver syndromeAutosomal dominant · Autosomal recessive
- ADCY5-related dyskinesiaAutosomal dominant
- Adenine phosphoribosyltransferase deficiencyAutosomal recessive
- Adenosine deaminase 2 deficiencyAutosomal recessive
- Adenosine deaminase deficiencyAutosomal recessive
- Adenosine monophosphate deaminase deficiencyAutosomal recessive
- Adenylosuccinate lyase deficiencyAutosomal recessive
- AdermatoglyphiaAutosomal dominant
- Adiposis dolorosaAutosomal dominant
- ADNP syndromeNot inherited
- Adolescent idiopathic scoliosisPattern unknown
- Adult polyglucosan body diseaseAutosomal recessive
- Adult-onset leukoencephalopathy with axonal spheroids and pigmented gliaAutosomal dominant
- African iron overloadPattern unknown
- Age-related hearing lossPattern unknown
- Age-related macular degenerationPattern unknown
- Aicardi syndromeX-linked dominant
- Aicardi-Goutières syndromeAutosomal recessive · Autosomal dominant
- Alagille syndromeAutosomal dominant
- Alcohol use disorderPattern unknown
- Aldosterone-producing adenomaNot inherited
- Alexander diseaseAutosomal dominant
- ALG1-congenital disorder of glycosylationAutosomal recessive
- ALG12-congenital disorder of glycosylationAutosomal recessive
- ALG6-congenital disorder of glycosylationAutosomal recessive
- AlkaptonuriaAutosomal recessive
- Allan-Herndon-Dudley syndromeX-linked recessive
- Allergic asthmaPattern unknown
- Alopecia areataPattern unknown
- Alpers-Huttenlocher syndromeAutosomal recessive
- Alpha thalassemiaPattern unknown
- Alpha thalassemia X-linked intellectual disability syndromeX-linked recessive
- Alpha-1 antitrypsin deficiencyAutosomal recessive
- Alpha-mannosidosisAutosomal recessive
- Alpha-methylacyl-CoA racemase deficiencyAutosomal recessive
- Alpha-N-acetylgalactosaminidase deficiencyAutosomal recessive
- Alport syndromeAutosomal recessive · Autosomal dominant · X-linked
- Alström syndromeAutosomal recessive
- Alternating hemiplegia of childhoodAutosomal dominant
- Alveolar capillary dysplasia with misalignment of pulmonary veinsAutosomal recessive · Autosomal dominant
- Alzheimer's diseasePattern unknown · Autosomal dominant, inherited from one affected parent
- Amelogenesis imperfectaAutosomal dominant · Autosomal recessive · X-linked
- Aminoacylase 1 deficiencyAutosomal recessive
- Amish lethal microcephalyAutosomal recessive
- Amyotrophic lateral sclerosisX-linked dominant · Not inherited · Autosomal dominant · Autosomal recessive
- Anauxetic dysplasiaAutosomal recessive
- Andermann syndromeAutosomal recessive
- Andersen-Tawil syndromeAutosomal dominant
- Androgen insensitivity syndromeX-linked recessive
- Androgenetic alopeciaPattern unknown
- AnencephalyPattern unknown
- Angelman syndromeNot inherited
- Anhidrotic ectodermal dysplasia with immune deficiencyAutosomal dominant · X-linked recessive
- AniridiaAutosomal dominant, inherited or a new variant
- Ankyloblepharon-ectodermal defects-cleft lip/palate syndromeAutosomal dominant
- Ankylosing spondylitisPattern unknown
- Ankyrin-B syndromeAutosomal dominant
- Anonychia congenitaAutosomal recessive
- Anophthalmia/MicrophthalmiaX-linked recessive · Autosomal dominant, or a new variant · Autosomal recessive · X-linked
- Anophthalmia/microphthalmia-esophageal atresia syndromeAutosomal dominant, or a new variant
- Antiphospholipid syndromePattern unknown
- Apert syndromeAutosomal dominant
- Arginase deficiencyAutosomal recessive
- Arginine vasopressin deficiencyAutosomal recessive · Autosomal dominant
- Arginine vasopressin resistanceAutosomal dominant · Autosomal recessive · X-linked
- Arginine:glycine amidinotransferase deficiencyAutosomal recessive
- Argininosuccinic aciduriaAutosomal recessive
- Aromatase deficiencyAutosomal recessive
- Aromatase excess syndromeAutosomal dominant
- Aromatic l-amino acid decarboxylase deficiencyAutosomal recessive
- Arrhythmogenic right ventricular cardiomyopathyAutosomal dominant · Autosomal recessive
- Arterial tortuosity syndromeAutosomal recessive
- Arts syndromeX-linked dominant
- Asparagine synthetase deficiencyAutosomal recessive
- AspartylglucosaminuriaAutosomal recessive
- Asphyxiating thoracic dystrophyAutosomal recessive
- Ataxia neuropathy spectrumAutosomal dominant · Autosomal recessive
- Ataxia with oculomotor apraxiaAutosomal recessive
- Ataxia with vitamin E deficiencyAutosomal recessive
- Ataxia-pancytopenia syndromeAutosomal dominant
- Ataxia-telangiectasiaAutosomal recessive
- Atelosteogenesis type 1Autosomal dominant
- Atelosteogenesis type 2Autosomal recessive
- Atelosteogenesis type 3Autosomal dominant
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