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Showing below up to 50 results in range #13,401 to #13,450.
- Aristolochic acid nephropathy (Q99409)
- Autosomal recessive spastic paraplegia type 24 (Q99408)
- Autosomal recessive spastic paraplegia type 30 (Q99407)
- Autosomal recessive spastic paraplegia type 14 (Q99406)
- Primary non-midline abdominal wall hernia (Q99405)
- Autosomal recessive spastic paraplegia type 20 (Q99404)
- Autosomal recessive spastic paraplegia type 18 (Q99403)
- Periorificial dermatitis of eyelids (Q99402)
- Autosomal recessive spastic paraplegia type 15 (Q99401)
- Autosomal recessive spastic paraplegia type 35 (Q99400)
- Pancreaticocutaneous fistula (Q99399)
- 9480/3 (Q99398)
- 9478/3 (Q99397)
- Autosomal recessive complex hereditary spastic paraplegia due to mutations in Spatacsin gene (Q99396)
- Autosomal recessive spastic paraplegia type 27 (Q99395)
- Autosomal recessive spastic paraplegia type 25 (Q99394)
- Autosomal recessive spastic paraplegia type 32 (Q99393)
- Autosomal recessive spastic paraplegia type 26 (Q99392)
- Aspergillus myocarditis (Q99391)
- Autosomal recessive spastic paraplegia type 23 (Q99390)
- Anterior tibialis tendinitis (Q99389)
- Acute bacterial myocarditis (Q99388)
- Protozoal myocarditis (Q99387)
- 9391/1 (Q99386)
- Helminthic myocarditis (Q99385)
- Posterior tibialis tendinitis (Q99384)
- Autosomal recessive spastic paraplegia type 39 (Q99383)
- Chronic bacterial myocarditis (Q99382)
- Mitochondrial 2-methylacetoacetyl-CoA thiolase deficiency, non potassium-stimulated (Q99381)
- Internal pancreatic fistula (Q99380)
- 9460/3 (Q99379)
- 9477/3 (Q99378)
- 9451/3 (Q99377)
- 9450/3 (Q99376)
- 9470/3 (Q99375)
- 9474/3 (Q99374)
- 9430/3 (Q99373)
- 9473/3 (Q99372)
- 9432/1 (Q99371)
- 9441/3 (Q99370)
- 9425/3 (Q99369)
- 9476/3 (Q99368)
- 9444/1 (Q99367)
- 9471/3 (Q99366)
- 9431/1 (Q99365)
- 9440/3 (Q99364)
- 9445/3 (Q99363)
- 9472/3 (Q99362)
- 9475/3 (Q99361)
- 9442/3 (Q99360)
