Disease Search
- Auditory Neuropathy
- Auditory neuropathy spectrum disorder
- Auditory neuropathy, autosomal dominant, 1
- Auditory Perceptual Disorder
- Aural atresia, congenital
- Aural cephalosyndactyly
- Auralcephalosyndactyly
- Auriculo-Condylar Syndrome
- Auriculoosteodysplasia
- Austin's disease
- Autism Spectrum Disorders
- Autistic disorder of childhood onset
- Autoimmune disease, syndromic multisystem
- Autoimmune Diseases
- Autoimmune Enteropathy
- Autoimmune gastrointestinal dysmotility
- Autoimmune Hemolytic Anemia
- Autoimmune Hepatitis
- Autoimmune Inner Ear disease
- Autoimmune Lymphoproliferative Syndrome
- Autoimmune lymphoproliferative syndrome, type 1a
- Autoimmune lymphoproliferative syndrome, type 1b
- Autoimmune lymphoproliferative syndrome, type 2
- Autoimmune lymphoproliferative syndrome, type IV
- Autoimmune Myocarditis
- Autoimmune Oophoritis
- Autoimmune Peripheral Neuropathy
- Autoimmune polyendocrinopathy-candidiasis–ectodermal dystrophy/dysplasia (APECED)
- Autoimmune Polyglandular Syndrome Type 1
- Autoimmune Polyglandular Syndrome Type 2
- Autoimmune Polyglandular Syndrome Type 3
- Autoimmune Progesterone Dermatitis
- Autoimmune retinopathy
- Autosomal Dominant
- Autosomal dominant centronuclear myopathy
- Autosomal Dominant Compelling Helio Ophthalmic Outburst Syndrome
- Autosomal dominant hyper IgE syndrome
- Autosomal dominant intellectual disability-6
- Autosomal dominant nocturnal frontal lobe epilepsy type 3
- Autosomal dominant optic atrophy
- Autosomal Dominant Partial Epilepsy with Auditory Features
- Autosomal dominant polycystic kidney disease
- Autosomal dominant polycystic liver disease
- Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 1
- Autosomal recessive Alport syndrome
- Autosomal recessive benign polycythemia
- Autosomal recessive centronuclear myopathy
- Autosomal recessive congenital ichthyosis, NIPAL4-related
- Autosomal recessive cutis laxa type 1
- Autosomal recessive cutis laxa type 2
- Autosomal recessive cytochrome b-negative
- Autosomal recessive hereditary thrombophilia due to protein C deficiency
- Autosomal recessive hyper IgE syndrome
- Autosomal recessive hypohidrotic ectodermal dysplasia syndrome
- Autosomal recessive hypophosphatemic bone disease
- Autosomal recessive hypophosphatemic rickets
- Autosomal recessive hypophosphatemic vitamin D refractory rickets
- Autosomal Recessive Nonsyndromic Congenital Nuclear Cataract
- Autosomal Recessive Polycystic Kidney Disease
- Autosomal recessive pseudohypoaldosteronism type 1
- Autosomal recessive spastic paraplegia type 21
- Autosomal recessive thrombophilia due to congenital protein C deficiency
- Autosomal recessive thrombophilia due to PC deficiency
- Avascular necrosis of femoral head, primary
- Avellino corneal dystrophy
- Avian flu
- Avian influenza
- Avoidant Personality Disorder
- Awakening epilepsy
- Axenfeld Rieger Syndrome Type 1
- Axenfeld Rieger Syndrome Type 2
- Axenfeld Rieger Syndrome Type 3
- Axenfeld-Rieger syndrome
- Axial Osteomalacia
- Azorean disease