Medical Encyclopedia: A
374 entries under “A”, projected from the canonical Medical Encyclopedia inventory. Index entries are listed by name while their full article is prepared and reviewed.
Educational information only. This explains health information to discuss with a qualified clinician; it is not a diagnosis, prescription, or treatment. Medical Information & Safety.
Showing 14 of 374 — page 7 of 7
- Autosomal dominant tubulointerstitial kidney disease-UMODDefinition and full article under review.
- Autosomal dominant vitreoretinochoroidopathyDefinition and full article under review.
- Autosomal Emery-Dreifuss Muscular DystrophyDefinition and full article under review.
- Autosomal recessive axonal neuropathy with neuromyotoniaDefinition and full article under review.
- Autosomal recessive cerebellar ataxia type 1Definition and full article under review.
- Autosomal recessive congenital methemoglobinemiaDefinition and full article under review.
- Autosomal recessive congenital stationary night blindnessDefinition and full article under review.
- Autosomal recessive hypotrichosisDefinition and full article under review.
- Autosomal recessive primary microcephalyDefinition and full article under review.
- Autosomal recessive spastic ataxia of Charlevoix-SaguenayDefinition and full article under review.
- AvitaminosisDefinition and full article under review.
- Axenfeld-Rieger syndromeDefinition and full article under review.
- Axial SpondyloarthritisDefinition and full article under review.
- AzoospermiaDefinition and full article under review.