Diseases List: N
List of diseases with information available on this website:
- N acetyltransferase deficiency
- N syndrome
- N-acetyl-alpha-D-galactosaminidase deficiency type III
- N-acetylaspartate deficiency
- N-acetylglutamate synthase deficiency
- N-acetylglutamate synthetase deficiency
- N-terminal acetyltransferase deficiency
- Nablus mask-like facial syndrome
- NADH cytochrome B5 reductase deficiency
- Naegeli syndrome
- Naegeli-Franceschetti-Jadassohn syndrome
- Naegeli-Franceschetti-Jadassohn syndrome/dermatopathia pigmentosa reticularis
- Naegleria fowleri
- Nager acrofacial dysostosis
- Nager syndrome
- Naguib-Richieri-Costa syndrome
- Nail bed telangiectasia
- Nail disorder
- Nail disorder, nonsyndromic congenital, type 10
- Nail disorder, nonsyndromic congenital, type 8
- Nail dysplasia, isolated congenital
- Nail Infection
- Nail-patella syndrome
- Nairobi Sheep Disease
- Nairovirus
- Nakajo syndrome
- Nakajo-Nishimura syndrome
- Nance-Horan syndrome
- Nanomaterial Exposure
- Nanophthalmos type 1
- Nanophthalmos type 2
- Naproxen response
- Narcissistic personality disorder
- Narcolepsy
- Narcolepsy type 1
- Narcolepsy type 2, susceptibility to
- Narcolepsy type 3
- Narcolepsy type 4, susceptibility to
- Narcolepsy type 5, susceptibility to
- Narcolepsy type 7
- Narrow greater sacrosciatic notches
- Narrow oral fissure short stature cone shaped epiphyses
- Narrow sacroiliac notch
- Narrow vertebral interpedicular distance
- Nasal and sinus cancer
- Nasal cancer
- Nasal Cavity Adenocarcinoma
- Nasal Cavity and Paranasal Sinus Neoplasm
- Nasal Cavity and Paranasal Sinus Squamous Cell Carcinoma
- Nasal Cavity Carcinoma
- Nasal Cavity Lymphoma
- Nasal Cavity Neoplasm
- Nasal Cavity Squamous Cell Carcinoma
- Nasal polyposis
- Nasal Polyps
- Nasodigitoacoustic syndrome
- Nasolacrimal duct obstruction
- Nasopalpebral lipoma coloboma syndrome
- Nasopharyngeal Cancer
- Nasopharyngeal carcinoma
- Nasopharyngeal Nonkeratinizing Carcinoma
- Nasopharyngeal Undifferentiated Carcinoma
- Nasopharyngitis
- Nasopharynx carcinoma
- Nasu-Hakola disease
- Natal teeth, intestinal pseudoobstruction and patent ductus
- Natal tooth
- Nathalie syndrome
- Native American myopathy
- Natural killer cell and glucocorticoid deficiency with DNA repair defect
- Natural killer cell deficiency
- Navajo neurohepatopathy
- Naxos disease
- NCI CTEP SDC Reproductive System Neoplasm Female Category Terminology
- Necatoriasis
- Neck arthritis
- Neck cancer
- Neck Carcinoma
- Neck Disorders
- Neck Dissection
- Neck fracture
- Neck injury
- Neck Neoplasm
- Neck strain
- Necrobiosis lipoidica
- Necrobiotic Disorders
- Necrobiotic xanthogranuloma
- Necrolytic Migratory Erythema
- Necrosis
- Necrotic Uveal Melanoma
- Necrotizing enterocolitis
- Necrotizing fasciitis
- Necrotizing gingivitis
- Necrotizing soft tissue infection
- Needle stick injury
- Needlestick injury
- Negative rheumatoid factor polyarthritis
- Neglect
- Neglected diseases
- Neglected Tropical Diseases
- Neisseria gonorrhoeae
- Neisseria meningitidis
- Neisseriaceae Infections
- Nelfinavir response
- Nelson syndrome
- Nemaline bodies
- Nemaline myopathy
- Nemaline myopathy type 1
- Nemaline myopathy type 10
- Nemaline myopathy type 2
- Nemaline myopathy type 3
- Nemaline myopathy type 4
- Nemaline myopathy type 5
- Nemaline myopathy type 6
- Nemaline myopathy type 7
- Nemaline myopathy type 8
- Nemaline myopathy type 9
- Nematode diseases
- NEMO Mutation Diseases
- Neocortical epilepsy
- Neoehrlichia mikurensis
- Neoehrlichiosis
- Neonatal abstinence syndrome
- Neonatal adrenoleucodystrophy
- Neonatal adrenoleukodystrophy
- Neonatal anemia
- Neonatal Behçet's disease
- Neonatal brain injury
- Neonatal Candidiasis
- Neonatal cardiorespiratory failure
- Neonatal chlamydia
- Neonatal conjunctivitis
- Neonatal death
- Neonatal Dengue
- Neonatal diabetes
- Neonatal diabetes mellitus
- Neonatal Disorders
- Neonatal encephalopathy
- Neonatal epiphyseal stippling
- Neonatal gonorrhea
- Neonatal Hemochromatosis
- Neonatal hepatitis
- Neonatal herpes
- Neonatal HSV
- Neonatal Hypoglycemia
- Neonatal hypothyroidism
- Neonatal hypotonia
- Neonatal intrahepatic cholestasis caused by citrin deficiency
- Neonatal jaundice
- Neonatal liver diseases
- Neonatal lupus
- Neonatal Marfan syndrome
- Neonatal meningitis
- Neonatal myasthenia
- Neonatal Onset Multisystem Inflammatory Disease
- Neonatal ovarian cyst
- Neonatal progeroid syndrome
- Neonatal pseudo-hydrocephalic progeroid syndrome
- Neonatal respiratory distress
- Neonatal respiratory distress syndrome
- Neonatal sepsis
- Neonatal severe hyperparathyroidism
- Neonatal short-limb short stature
- Neonatal Sjögren's syndrome
- Neonatal stroke
- Neonatal syphilis
- Neonatal systemic lupus erythematosus
- Neonatal Withdrawal Syndrome
- Neoplasm of Uncertain Malignant Potential
- Neoplasm Recurrence, Local
- Neoplasms
- Neoplasms, Basal Cell
- Neoplasms, Complex and Mixed
- Neoplasms, Multiple Primary
- Neoplastic diseases
- Neoplastic Post-Transplant Lymphoproliferative Disorder
- Neoplastic Pregnancy Complications
- Neoplastic Processes
- Neoplastic Stem Cells
- Neovascular AMD
- Neovascular glaucoma
- Neovascularization of peripheral and posterior retina
- Nephritis
- Nephroblastoma
- Nephroblastomatosis
- Nephrocalcinosis
- Nephrogenic diabetes insipidus
- Nephrogenic diabetes insipidus, autosomal
- Nephrogenic diabetes insipidus, X-linked
- Nephrogenic Fibrosing Dermopathy
- Nephrogenic rest
- Nephrogenic syndrome of inappropriate antidiuresis
- Nephrogenic Systemic Fibrosis
- Nephrolithiasis
- Nephrolithiasis/osteoporosis, hypophosphatemic, type 1
- Nephrolithiasis/osteoporosis, hypophosphatemic, type 2
- Nephronophthisis
- Nephronophthisis type 1
- Nephronophthisis type 11
- Nephronophthisis type 12
- Nephronophthisis type 13
- Nephronophthisis type 14
- Nephronophthisis type 15
- Nephronophthisis type 16
- Nephronophthisis type 18
- Nephronophthisis type 19
- Nephronophthisis type 4
- Nephronophthisis type 7
- Nephronophthisis type 8
- Nephronophthisis type 9
- Nephronophthisis-like nephropathy type 1
- Nephropathic cystinosis
- Nephropathy
- Nephropathy with pretibial epidermolysis bullosa and deafness
- Nephropathy, deafness, and hyperparathyroidism
- Nephroptosis
- Nephrosclerosis
- Nephrosis
- Nephrosis deafness urinary tract digital malformation
- Nephrotic range proteinuria
- Nephrotic Syndrome
- Nephrotic Syndrome in Children
- Nephrotic syndrome ocular anomalies
- Nephrotic syndrome, idiopathic, steroid-resistant
- Nephrotic syndrome, type 10
- Nephrotic syndrome, type 3
- Nephrotic syndrome, type 5, with or without ocular abnormalities
- Nephrotic syndrome, type 6
- Nephrotic syndrome, type 7
- Nephrotic syndrome, type 8
- Nephrotic syndrome, type 9
- Nerve agent exposure
- Nerve block
- Nerve compression
- Nerve damage
- Nerve Disorders
- Nerve entrapment
- Nerve entrapment syndromes
- Nerve injury
- Nerve Plexus Neoplasm
- Nerve root compression
- Nerve root disorders
- Nerve Root Neoplasm
- Nerve Tissue Neoplasms
- Nervous system benign neoplasm
- Nervous system cancer
- Nervous System Disorders
- Nervous system neoplasm
- Nervous System Trauma
- Nervous system tumors
- Nestor-guillermo progeria syndrome
- Netherton syndrome
- Neu Laxova syndrome
- Neu-Laxova syndrome type 1
- Neu-laxova syndrome type 2
- Neuhauser Daly Magnelli syndrome
- Neuhauser Eichner Opitz syndrome
- Neural crest tumor
- Neural Tube Defects
- Neural tube defects, folate-sensitive
- Neuralgia
- Neurally Mediated Hypotension
- Neurally Mediated Syncope
- Neuraminidase Deficiency
- Neurilemmoma
- Neuritis
- Neuroacanthocytosis
- Neuroaspergillosis
- Neuroaxonal dystrophy
- Neuroaxonal dystrophy renal tubular acidosis
- Neuroaxonal dystrophy, infantile
- Neurobehavioral Manifestations
- Neuroblastoma
- Neuroblastoma type 1
- Neuroblastoma type 2
- Neuroblastoma type 3
- Neuroborreliosis
- Neurocognitive Disorders
- Neurocutaneous melanosis
- Neurocutaneous Syndromes
- Neurocysticercosis
- Neurocytoma
- Neurodegeneration
- Neurodegeneration with brain iron accumulation
- Neurodegeneration With Brain Iron Accumulation type 1
- Neurodegeneration With Brain Iron Accumulation Type 2a
- Neurodegeneration with brain iron accumulation type 2b
- Neurodegeneration With Brain Iron Accumulation Type 3
- Neurodegeneration with brain iron accumulation type 4
- Neurodegeneration with brain iron accumulation type 5
- Neurodegeneration with brain iron accumulation type 6
- Neurodegeneration with optic atrophy, childhood-onset
- Neurodegenerative diseases
- Neurodermatitis
- Neurodevelopmental disorders
- Neuroectodermal Tumor
- Neuroendocrine carcinoma
- Neuroendocrine carcinoma of the cervix
- Neuroendocrine disorders
- Neuroendocrine neoplasm
- Neuroendocrine tumors
- Neuroepithelial Neoplasm
- Neuroepithelioma
- Neurofaciodigitorenal syndrome
- Neuroferritinopathy
- Neurofibroma
- Neurofibromatosis
- Neurofibromatosis Type 1
- Neurofibromatosis Type 2
- Neurofibromatosis type 3A
- Neurofibromatosis type 4
- Neurofibromatosis, familial spinal
- Neurofibromatosis, type III, mixed central and peripheral
- Neurofibromatosis-Noonan syndrome
- Neurofibromatosis-pheochromocytoma-duodenal carcinoid syndrome
- Neurofibrosarcoma
- Neurogenic arthrogryposis multiplex congenita
- Neurogenic bladder
- Neurogenic Communication Disorder
- Neurogenic shock
- Neurogenic stuttering
- Neurogenic Thoracic Outlet Syndrome
- Neurohypophyseal diabetes insipidus
- Neuroleptic Malignant Syndrome
- Neurologic Angiostrongyliasis
- Neurologic Channelopathies
- Neurologic Gait Disorders
- Neurologic Manifestations
- Neurologic neglect syndrome
- Neurologic Waardenburg-Shah syndrome
- Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset
- Neurological Disorders
- Neurological speech impairment
- Neuroma
- Neurometabolic diseases
- Neuromuscular diseases
- Neuromuscular Disorders
- Neuromuscular Manifestations
- Neuromyelitis optica
- Neuromyelitis optica spectrum disorder
- Neuromyotonia and axonal neuropathy, autosomal recessive
- Neuronal ceroid lipofuscinoses
- Neuronal ceroid lipofuscinosis
- Neuronal ceroid lipofuscinosis 8 northern epilepsy variant
- Neuronal ceroid lipofuscinosis type 10
- Neuronal ceroid lipofuscinosis type 2
- Neuronal ceroid lipofuscinosis type 3
- Neuronal ceroid lipofuscinosis type 5
- Neuronal ceroid lipofuscinosis type 6
- Neuronal ceroid lipofuscinosis type 7
- Neuronal ceroid lipofuscinosis type 9
- Neuronal intestinal dysplasia, type b
- Neuronal intranuclear inclusion disease
- Neuronal loss in basal ganglia
- Neuronal loss in central nervous system
- Neuronal Migration Disorders
- Neuronopathy, distal hereditary motor, type I
- Neuronopathy, distal hereditary motor, type viia
- Neuropathy
- Neuropathy ataxia retinitis pigmentosa syndrome
- Neuropathy hereditary sensory and autonomic type 1
- Neuropathy pain
- Neuropathy, Ataxia and Retinitis Pigmentosa Syndrome
- Neuropathy, ataxia, and retinitis pigmentosa
- Neuropathy, congenital, with arthrogryposis multiplex
- Neuropathy, distal hereditary motor, Jerash type
- Neuropathy, hereditary motor and sensory, Okinawa type
- Neuropathy, hereditary motor and sensory, Russe type
- Neuropathy, Hereditary Motor And Sensory, Type VIB
- Neuropathy, Hereditary Sensory And Autonomic, Type II
- Neuropathy, hereditary sensory and autonomic, type VI
- Neuropathy, hereditary sensory and autonomic, type VII
- Neuropathy, hereditary sensory and autonomic, type VIII
- Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive
- Neuropsychiatric disorders
- Neurosarcoidosis
- Neuroschistosomiasis
- Neurosis
- Neurosyphilis
- Neurothekeoma
- Neurotic disorders
- Neurotoxic Shellfish Poisoning
- Neurotoxicity
- Neurotrophic keratitis
- Neutral 1 amino acid transport defect
- Neutral lipid storage disease
- Neutral lipid storage disease with myopathy
- Neutropenia
- Neutropenia chronic familial
- Neutropenia lethal congenital with eosinophilia
- Neutropenia, nonimmune chronic idiopathic, of adults
- Neutropenia, Severe Congenital, 4, Autosomal Recessive
- Neutropenic Fever
- Neutrophil immunodeficiency syndrome
- Neutrophil-specific granule deficiency
- Nevi and Melanomas
- Nevi flammei, familial multiple
- Nevoid basal cell carcinoma syndrome
- Nevus
- Nevus Anemicus
- Nevus comedonicus
- Nevus comedonicus syndrome
- Nevus of Ito
- Nevus of Ota
- Nevus sebaceous
- New Daily Persistent Headache
- New Psychoactive Substances
- Newborn jaundice
- Newborn respiratory distress syndrome
- Newborn Screening Disorders
- Newcastle Disease
- Newfoundland rod-cone dystrophy
- NF-kappa B
- NF-kappa B Essential Modulator Deficiency
- NF1-microdeletion syndrome
- Nguyen syndrome
- Nickel Allergy
- Nickel poisoning
- Nicolaides-Baraitser syndrome
- Nicotine
- Nicotine Addiction
- Nicotine Dependence
- Nicotine Intoxication
- Nicotine Poisoning
- Nicotine withdrawal
- Niemann-Pick Disease
- Niemann-Pick disease type A
- Niemann-Pick disease type B
- Niemann-Pick disease type C
- Niemann-Pick disease type C1
- Niemann-Pick disease type C2
- Niemann-Pick disease type D
- Niemann-pick disease, intermediate, protracted neurovisceral
- Nievergelt syndrome
- Nifedipine response
- Night Blindness
- Night blindness skeletal anomalies unusual facies
- Night blindness, congenital stationary, type 1g
- Night terrors
- Nightmares
- Nijmegen breakage syndrome
- Nijmegen breakage syndrome-like disorder
- Nilotinib response
- Nipah virus
- Nipah virus encephalitis
- Nipple abscess
- Nipple Cancer
- Nipple Carcinoma
- Nipple Disorders
- Nipple eczema
- Nipple herpes
- Nipple Neoplasm
- Nipple Yeast Infection
- Nitrite Abuse
- Nitrogen Mustard exposure
- Noble Bass Sherman syndrome
- Nocardiosis
- Nociceptive Pain
- Nocturia
- Nocturnal Enuresis
- Nodal marginal zone lymphoma
- NODAL-Related Holoprosencephaly
- Nodding syndrome
- Nodular Acne
- Nodular fasciitis
- Nodular goiter
- Nodular Hidradenoma
- Nodular melanoma
- Nodular nonsuppurative panniculitis
- Nodular regenerative hyperplasia
- Noise injury
- Noise-Induced Hearing Loss
- Noma
- Non-24-hour sleep wake disorder
- Non-A-E hepatitis
- Non-alcoholic fatty liver disease
- Non-cardia gastric cancer
- Non-Classic Congenital Adrenal Hyperplasia
- Non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency
- Non-communicating hydrocephalus
- Non-Cutaneous Leiomyosarcoma
- Non-distal trisomy 10q
- Non-distal trisomy 13q
- Non-dystrophic myotonic disorders
- Non-Epileptic Seizures
- Non-fluent aphasia
- Non-functioning pancreatic endocrine tumor
- Non-functioning pituitary adenoma
- Non-Functioning Pituitary Gland Neoplasm
- Non-Gestational Ovarian Choriocarcinoma
- Non-Hodgkin lymphoma, during pregnancy
- Non-Hodgkin’s Lymphoma
- Non-immune hydrops fetalis
- Non-infectious uveitis
- Non-insulinoma pancreatogenous hypoglycemia syndrome
- Non-involuting congenital hemangioma
- Non-ketotic hyperglycinemia
- Non-Langerhans-Cell Histiocytosis
- Non-midline cleft lip
- Non-Neoplastic Endocrine Disorder
- Non-Neoplastic Skin Disorder
- Non-papillary transitional cell carcinoma of the urinary bladder
- Non-polio enteroviruses
- Non-Q-Wave Myocardial Infarction
- Non-rhizomelic chondrodysplasia punctata
- Non-segmental vitiligo
- Non-seminoma germ cell tumor
- Non-seminoma testicular cancer
- Non-small cell lung cancer
- Non-Specific Urethritis
- Non-suppurative otitis media
- Non-syndromic genetic deafness
- Non-syndromic X-linked intellectual disability
- Non-traumatic osteonecrosis
- Nonaka myopathy
- Nonalcoholic fatty liver disease
- Nonalcoholic steatohepatitis
- Nonarteritic anterior ischemic optic neuropathy
- Nonarteritic anterior ischemic optic neuropathy, susceptibility to
- Nonbacterial prostatitis
- Nonbullous congenital ichthyosiform erythroderma
- Noncompaction cardiomyopathy
- Nondystrophic myotonia
- Nonepidemic Gay-related Kaposi Sarcoma
- Nonepidermolytic palmoplantar keratoderma
- Nonfunctioning pituitary tumors
- Nongerminomas
- Nongonococcal urethritis
- Nonimmune hydrops fetalis
- Nonmedullary thyroid carcinoma, with or without cell oxyphilia
- Nonmotile sperm
- Nonossified fifth metatarsal
- Nonpersistence of intestinal lactase
- Nonprogressive cerebellar ataxia
- Nonprogressive encephalopathy
- Nonprogressive restrictive external ophthalmoplegia
- Nonseminoma
- Nonspecific Interstitial Pneumonia
- Nonspherocytic hemolytic anemia
- Nonspherocytic hemolytic anemia due to hexokinase deficiency
- Nonsyndromic aplasia cutis congenita
- Nonsyndromic Deafness
- Nonsyndromic hearing loss
- Nonsyndromic Hereditary Hearing Impairment
- Nonsyndromic hereditary sensorineural hearing loss
- Nonsyndromic holoprosencephaly
- Nonsyndromic microcephaly
- Nonsyndromic paraganglioma
- Nonteratogenic Effects
- Nontuberculous mycobacterial lung disease
- Nontuberculous Mycobacterium Infections
- Nontuberculous Mycobacterium Pulmonary Disease
- Nontyphoidal Salmonellosis
- Noonan syndrome
- Noonan syndrome type 1
- ...and more....
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