List of diseases (N)
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This is a list of diseases starting with the letter "N".
N–Nas
- N acetyltransferase deficiency
- N syndrome
- N-Acetylglutamate synthase deficiency
- N-acetyl-alpha-D-galactosaminidase
- N-acetyl-glucosamine-6-sulfate sulfatase deficiency
- NADH CoQ reductase, deficiency of
- NADH cytochrome B5 reductase deficiency
- Naegeli–Franceschetti–Jadassohn syndrome
- Naguib syndrome
- Nail–patella syndrome
- Nakajo–Nishimura syndrome
- Nakajo syndrome
- Nakamura–Osame syndrome
- NAME syndrome
- Nance–Horan syndrome
- Nanism due to growth hormone combined deficiency
- Nanism due to growth hormone isolated deficiency with X-linked hypogammaglobulinemia
- Nanism due to growth hormone resistance
- Narcissistic personality disorder
- Narcolepsy
- Narrow oral fissure short stature cone shaped epiphyses
- Nasodigitoacoustic syndrome
- Nasopalpebral lipoma coloboma syndrome
- Nasopharyngeal carcinoma
- Nasopharyngeal teratoma Dandy–Walker diaphragmatic hernia
- Nasopharyngitis
Nat–Nav
Ne
Nec–Neo
- Necrotizing arteriolitis
- Necrotizing encephalopathy, infantile subacute
- Necrotizing enterocolitis
- Necrotizing fasciitis
- Necrotizing pneumonia
- Negative rheumatoid factor polyarthritis
- Neisseria meningitidis
- Nelson syndrome
- Nemaline myopathy
- Neonatal diabetes mellitus
- Neonatal hemochromatosis
- Neonatal hepatitis
- Neonatal infection
- Neonatal herpes
- Neonatal ovarian cyst
- Neonatal transient jaundice
Nep–Net
- Nephroblastomatosis, fetal ascites, macrosomia and Wilms' tumor
- Nephrocalcinosis
- Nephrogenic diabetes insipidus
- Nephrolithiasis type 2
- Nephronophthisis familial adult spastic quadriparesis
- Nephropathy deafness hyperparathyroidism
- Nephropathy familial with hyperuricemia
- Nephropathy, familial with gout
- Nephrosclerosis
- Nephrosis deafness urinary tract digital malformation
- Nephrosis neuronal dysmigration syndrome
- Nephrotic syndrome
- Nephrotic syndrome ocular anomalies
- Nephrotic syndrome, idiopathic, steroid-resistant
- Nerve sheath neoplasm
- Nesidioblastosis of pancreas
- Netherton syndrome ichthyosis
Neu
Neuh
Neur
Neura–Neuri
Neuro
Neuroa–Neurog
- Neuroacanthocytosis
- Neuroaxonal dystrophy renal tubular acidosis
- Neuroaxonal dystrophy, late infantile
- Neuroblastoma
- Neurocutaneous melanosis
- Neurocysticercosis
- Neuroectodermal endocrine syndrome
- Neuroectodermal tumors primitive
- Neuroendocrine cancer
- Neuroendocrine carcinoma of the cervix
- Neuroendocrine tumor
- Neuroepithelioma
- Neurofaciodigitorenal syndrome
- Neurofibrillary tangles
- Neurofibroma
- Neurofibromatosis
- Neurofibrosarcoma
- Neurogenic hypertension
Neurol–Neurot
- Neuroleptic malignant syndrome
- Neuroma biliary tract
- Neuromyotonia
- Neuronal ceroid lipofuscinosis
- Neuronal heterotopia
- Neuronal interstitial dysplasia
- Neuronal intestinal pseudoobstruction
- Neuronal intranuclear hyaline inclusion disease
- Neuronal intranuclear inclusion disease
- Neuropathy ataxia and retinitis pigmentosa
- Neuropathy congenital sensory neurotrophic keratitis
- Neuropathy hereditary with liability to pressure palsies
- Neuropathy motor sensory type 2 deafness mental retardation
- Neuropathy sensory spastic paraplegia
- Neuropathy, hereditary motor and sensory, LOM type
- Neuropathy, hereditary sensory, type I
- Neuropathy, hereditary sensory, type II
- Neurosyphilis
- Neurotoxicity syndromes
Neut
Nev–Nez
Ni–Nm
No
Noa–Nor
- Noah syndrome
- Noble–Bass–Sherman syndrome
- Nocardiosis
- Noise-induced hearing loss
- Noma
- Non-24-hour sleep–wake disorder
- Non functioning pancreatic endocrine tumor
- Nonallergic atopic dermatitis
- Non-Hodgkin lymphoma
- Noninsulin-dependent diabetes mellitus with deafness
- Nonketotic hyperglycinemia
- Non-lissencephalic cortical dysplasia
- Nonmedullary thyroid carcinoma, with cell oxyphilia
- Nonne–Milroy disease
- Non-small cell lung cancer
- Nonimmune hydrops fetalis
- Nonsyndromic hereditary hearing impairment
- Nonvenereal endemic syphilis
- Nonverbal learning disorder
- Noonan like syndrome
- Noonan syndrome
- Norman–Roberts lissencephaly syndrome
- Normokalemic periodic paralysis
- Norrie disease
- Northern epilepsy syndrome
- Norum disease
Nos–Nov
Nu–Ny
References
- ↑ Di Ferrante, Nicola (1980-10-24). "N -Acetylglucosamine-6-Sulfate Sulfatase Deficiency Reconsidered". Science. 210 (4468): 448. Bibcode:1980Sci...210..448D. doi:10.1126/science.6776626. ISSN 0036-8075. PMID 6776626.
- ↑ Koopman, R. J.; Happle, R. (1991). "Autosomal dominant transmission of the NAME syndrome (nevi, atrial myxoma, mucinosis of the skin and endocrine overactivity)". Human Genetics. 86 (3): 300–304. doi:10.1007/BF00202415. ISSN 0340-6717. PMID 1997386.
- ↑ Slowik, Jennifer M.; Collen, Jacob F.; Yow, Allison G. (2026), "Narcolepsy", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 29083681, retrieved 2026-08-23
- ↑ Jennette, J. C.; Falk, R. J.; Bacon, P. A.; Basu, N.; Cid, M. C.; Ferrario, F.; Flores-Suarez, L. F.; Gross, W. L.; Guillevin, L.; Hagen, E. C.; Hoffman, G. S.; Jayne, D. R.; Kallenberg, C. G. M.; Lamprecht, P.; Langford, C. A. (2013). "2012 revised International Chapel Hill Consensus Conference Nomenclature of Vasculitides". Arthritis and Rheumatism. 65 (1): 1–11. doi:10.1002/art.37715. ISSN 1529-0131. PMID 23045170.
- ↑ Ginglen, Jacob G.; Butki, Nikolai (2026), "Necrotizing Enterocolitis", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 30020729, retrieved 2026-08-22
- ↑ Wallace, Heather A.; Perera, Thomas B. (2026), "Necrotizing Fasciitis", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 28613507, retrieved 2026-08-22
- ↑ Kapania, Esha Madhu; Cavallazzi, Rodrigo (2024-11-10). "Necrotizing Pneumonia: A Practical Guide for the Clinician". Pathogens. 13 (11): 984. doi:10.3390/pathogens13110984. ISSN 2076-0817. PMC 11597800. PMID 39599537.
- ↑ Monserrate, Andres E.; De Jesus, Orlando (2026), "Nelson Syndrome", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 32809590, retrieved 2026-08-22
- ↑ Meyrier, Alain (2015). "Nephrosclerosis: a term in quest of a disease". Nephron. 129 (4): 276–282. doi:10.1159/000381195. ISSN 2235-3186. PMID 25871843.
- ↑ Tapia, Carolina; Bashir, Khalid (2026), "Nephrotic Syndrome", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 29262216, retrieved 2026-08-22
- ↑ Conti, Piero; Pansini, Gastone; Mouchaty, Homere; Capuano, Christian; Conti, Renato (2004). "Spinal neurinomas: retrospective analysis and long-term outcome of 179 consecutively operated cases and review of the literature". Surgical Neurology. 61 (1): 34–43, discussion 44. doi:10.1016/s0090-3019(03)00537-8. ISSN 0090-3019. PMID 14706374.
- ↑ Thomas, G. H.; Goldberg, M. F.; Miller, C. S.; Reynolds, L. W. (1979). "Neuraminidase deficiency in the original patient with the Goldberg syndrome". Clinical Genetics. 16 (5): 323–330. doi:10.1111/j.1399-0004.1979.tb01010.x. ISSN 0009-9163. PMID 519904.
- ↑ Maris, John M.; Hogarty, Michael D.; Bagatell, Rochelle; Cohn, Susan L. (2007-06-23). "Neuroblastoma". Lancet. 369 (9579). London, England: 2106–2120. Bibcode:2007Lanc..369.2106M. doi:10.1016/S0140-6736(07)60983-0. ISSN 1474-547X. PMID 17586306.
- ↑ Del Brutto, Oscar H. (2014). "Neurocysticercosis". The Neurohospitalist. 4 (4): 205–212. doi:10.1177/1941874414533351. ISSN 1941-8744. PMC 4212415. PMID 25360206.
- ↑ Mikami, Taro; Honma-Koretsune, Yuki; Tsunoda, Yui; Kagimoto, Shintaro; Yabuki, Yuichiro; Maegawa, Jiro; Terauchi, Takashi; Nawata, Shintaro; Kamide, Hiroyuki; Ishiwata, Yoshinobu; Kino, Tabito; Sugano, Teruyasu (2020-05-18). "Cardiac overload resolved by resection of a large plexiform neurofibroma on both the buttocks and upper posterior thighs in a patient with neurofibromatosis type I: a case report". BMC Surgery. 20 (1): 106. doi:10.1186/s12893-020-00761-4. ISSN 1471-2482. PMC 7236506. PMID 32423401.
- ↑ al-Gazali, L. I.; Bakalinova, D.; Varady, E.; Scorer, J.; Nork, M. (1997). "Further delineation of Nevo syndrome". Journal of Medical Genetics. 34 (5): 366–370. doi:10.1136/jmg.34.5.366. ISSN 0022-2593. PMC 1050942. PMID 9152832.
- ↑ Pearse, Gail (2006). "Normal structure, function and histology of the thymus". Toxicologic Pathology. 34 (5): 504–514. doi:10.1080/01926230600865549. ISSN 0192-6233. PMID 17067941.
- ↑ Bajwa, Hamza; Azhar, Waqas (2026), "Niemann-Pick Disease", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 32310589, retrieved 2026-08-22
- ↑ Saldarriaga-Cantillo, Alejandra; Rivas Nieto, Juan Carlos (2015). "Noah syndrome: a variant of Diogenes syndrome accompanied by animal hoarding practices". Journal of Elder Abuse & Neglect. 27 (3): 270–275. doi:10.1080/08946566.2014.978518. ISSN 1540-4129. PMID 25397353.
- ↑ Rawat, Deepa; Rajasurya, Venkat; Chakraborty, Rebanta K.; Sharma, Sandeep (2023), "Nocardiosis", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 30252331, retrieved 2026-10-17
- ↑ Auger, R. Robert; Burgess, Helen J.; Emens, Jonathan S.; Deriy, Ludmila V.; Thomas, Sherene M.; Sharkey, Katherine M. (2015-10-15). "Clinical Practice Guideline for the Treatment of Intrinsic Circadian Rhythm Sleep-Wake Disorders: Advanced Sleep-Wake Phase Disorder (ASWPD), Delayed Sleep-Wake Phase Disorder (DSWPD), Non-24-Hour Sleep-Wake Rhythm Disorder (N24SWD), and Irregular Sleep-Wake Rhythm Disorder (ISWRD). An Update for 2015: An American Academy of Sleep Medicine Clinical Practice Guideline". Journal of Clinical Sleep Medicine: JCSM: Official Publication of the American Academy of Sleep Medicine. 11 (10): 1199–1236. doi:10.5664/jcsm.5100. ISSN 1550-9397. PMC 4582061. PMID 26414986.
- ↑ Coughlin, Curtis R.; Swanson, Michael A.; Kronquist, Kathryn; Acquaviva, Cécile; Hutchin, Tim; Rodríguez-Pombo, Pilar; Väisänen, Marja-Leena; Spector, Elaine; Creadon-Swindell, Geralyn; Brás-Goldberg, Ana M.; Rahikkala, Elisa; Moilanen, Jukka S.; Mahieu, Vincent; Matthijs, Gert; Bravo-Alonso, Irene (2017). "The genetic basis of classic nonketotic hyperglycinemia due to mutations in GLDC and AMT". Genetics in Medicine: Official Journal of the American College of Medical Genetics. 19 (1): 104–111. doi:10.1038/gim.2016.74. ISSN 1530-0366. PMID 27362913.
- ↑ Vanaparthy, Rachana; Vadakekut, Elsa S.; Mahdy, Heba (2026), "Nonimmune Hydrops Fetalis", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 33085361, retrieved 2026-08-22
- ↑ Sloan-Heggen, Christina M.; Bierer, Amanda O.; Shearer, A. Eliot; Kolbe, Diana L.; Nishimura, Carla J.; Frees, Kathy L.; Ephraim, Sean S.; Shibata, Seiji B.; Booth, Kevin T.; Campbell, Colleen A.; Ranum, Paul T.; Weaver, Amy E.; Black-Ziegelbein, E. Ann; Wang, Donghong; Azaiez, Hela (2016). "Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss". Human Genetics. 135 (4): 441–450. doi:10.1007/s00439-016-1648-8. ISSN 1432-1203. PMC 4796320. PMID 26969326.
- ↑ Mitjà, Oriol; Šmajs, David; Bassat, Quique (2013). "Advances in the diagnosis of endemic treponematoses: yaws, bejel, and pinta". PLOS Neglected Tropical Diseases. 7 (10) e2283. Bibcode:2013PNTDi...7e2283M. doi:10.1371/journal.pntd.0002283. ISSN 1935-2735. PMC 3812090. PMID 24205410.
- ↑ Anderson, Kailyn; Cnota, James; James, Jeanne; Miller, Erin M.; Parrott, Ashley; Pilipenko, Valentina; Weaver, Kathryn Nicole; Shikany, Amy (2019). "Prevalence of Noonan spectrum disorders in a pediatric population with valvar pulmonary stenosis". Congenital Heart Disease. 14 (2): 264–273. doi:10.1111/chd.12721. ISSN 1747-0803. PMID 30556322.
- ↑ Hong, S. E.; Shugart, Y. Y.; Huang, D. T.; Shahwan, S. A.; Grant, P. E.; Hourihane, J. O.; Martin, N. D.; Walsh, C. A. (2000). "Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations". Nature Genetics. 26 (1): 93–96. doi:10.1038/79246. ISSN 1061-4036. PMID 10973257.
- ↑ Warburg, M. (1971). "Norrie's disease". Birth Defects Original Article Series. 7 (3): 117–124. ISSN 0547-6844. PMID 5006136.
- ↑ Midun, Elise; Radulovic, Suzana; Brough, Helen; Caubet, Jean-Christoph (2021). "Recent advances in the management of nut allergy". The World Allergy Organization Journal. 14 (1) 100491. doi:10.1016/j.waojou.2020.100491. ISSN 1939-4551. PMC 7811165. PMID 33510829.
- ↑ Kaur, Kirandeep; Rocha Cabrero, Franklyn; Deibel, Jonathon P. (2025), "Nystagmus Types", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 30969533, retrieved 2026-10-17
