HealthSignal
Rare conditions starting with N
Every condition in the NIH Genetic and Rare Diseases Information Center has its own HealthSignal community page, with condition information, stories, research and Signals sign-up.
163 conditions starting with N
- N syndrome
- NAD(P)HX dehydratase deficiency
- Naegeli-Franceschetti-Jadassohn syndrome
- Nager syndrome
- Nail and teeth abnormalities-marginal palmoplantar keratoderma-oral hyperpigmentation syndrome
- Nail-patella syndrome
- Nail-patella-like renal disease
- Namaqualand hip dysplasia
- Nance-Horan syndrome
- Nanophthalmia
- Narcolepsy
- NARP syndrome
- Nasal cavity and paranasal sinus carcinoma
- Nasopalpebral lipoma-coloboma syndrome
- Nasopharyngeal carcinoma
- Nathalie syndrome
- Naxos disease
- NDE1-related microhydranencephaly
- Nebulin-related early-onset distal myopathy
- Necrobacillosis
- Necrobiosis lipoidica
- Necrobiotic xanthogranuloma
- Necrotizing enterocolitis
- Necrotizing soft tissue infection
- Necrotizing vasculitis
- NEK9-related lethal skeletal dysplasia
- Nelson syndrome
- Nemaline myopathy
- Nemaline myopathy 5
- Neonatal asphyxia
- Neonatal diabetes mellitus
- Neonatal diabetes mellitus with congenital hypothyroidism
- Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome
- Neonatal hemochromatosis
- Neonatal ichthyosis-sclerosing cholangitis syndrome
- Neonatal inflammatory skin and bowel disease
- Neonatal intrahepatic cholestasis due to citrin deficiency
- Neonatal Marfan syndrome
- Neonatal pseudo-hydrocephalic progeroid syndrome
- Neonatal severe primary hyperparathyroidism
- Neonatal-onset encephalopathy with rigidity and seizures
- Neoplasm of the pituitary gland
- Nephrogenic diabetes insipidus
- Nephrogenic diabetes insipidus-intracranial calcification syndrome
- Nephrogenic syndrome of inappropriate antidiuresis
- Nephrogenic systemic fibrosis
- Nephronophthisis
- Nephropathy - deafness - hyperparathyroidism syndrome
- Nephrosis-deafness-urinary tract-digital malformations syndrome
- Nestor-Guillermo progeria syndrome
- Netherton syndrome
- Neu-Laxova syndrome
- Neural tube defect
- Neural tube defects, X-linked
- Neuralgic amyotrophy
- Neurenteric cyst
- Neuroacanthocytosis
- Neuroaxonal dystrophy renal tubular acidosis
- Neuroblastoma
- Neurocutaneous melanocytosis
- Neurodegeneration with brain iron accumulation
- Neurodegeneration with brain iron accumulation 2B
- Neurodegeneration with brain iron accumulation 4
- Neurodegeneration with brain iron accumulation 5
- Neurodegeneration with brain iron accumulation 6
- Neurodevelopmental disorder with alopecia and brain abnormalities
- Neurodevelopmental disorder with dysmorphic facies and variable seizures
- Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination
- Neurodevelopmental disorder with hypotonia, brain anomalies, distinctive facies, and absent language
- Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies
- Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities
- Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities
- Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart
- Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant
- Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies
- Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities
- Neurodevelopmental disorder with severe motor impairment and absent language
- Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome
- Neuroectodermal melanolysosomal disease
- Neuroectodermal-endocrine syndrome
- Neuroendocrine neoplasm
- Neuroendocrine tumor of pancreas
- Neuroepithelioma
- Neurofaciodigitorenal syndrome
- Neuroferritinopathy
- Neurofibroma
- Neurofibromatosis
- Neurofibromatosis-Noonan syndrome
- Neurofibromatosis, type 1
- Neurofibromatosis, type 2
- Neurofibrosarcoma
- Neurogenic scapuloperoneal syndrome, Kaeser type
- Neuroleptic malignant syndrome
- Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 1
- Neuromuscular disease caused by qualitative or quantitative defects of dysferlin
- Neuromyelitis optica
- Neuronal ceroid lipofuscinosis
- Neuronal ceroid lipofuscinosis 1
- Neuronal ceroid lipofuscinosis 10
- Neuronal ceroid lipofuscinosis 2
- Neuronal ceroid lipofuscinosis 3
- Neuronal ceroid lipofuscinosis 5
- Neuronal ceroid lipofuscinosis 7
- Neuronal ceroid lipofuscinosis 8 northern epilepsy variant
- Neuronal ceroid lipofuscinosis 9
- Neuronal intranuclear inclusion disease
- Neuronopathy, distal hereditary motor, autosomal dominant 1
- Neuronopathy, distal hereditary motor, autosomal dominant 8
- Neuronopathy, distal hereditary motor, autosomal recessive 3
- Neuronopathy, distal hereditary motor, autosomal recessive 4
- Neuronopathy, distal hereditary motor, type 5
- Neuropathy with hearing impairment
- Neuropathy, hereditary sensory and autonomic, type 1A
- Neurosyphilis
- Neutral 1 amino acid transport defect
- Neutral lipid storage disease
- Neutral lipid storage myopathy
- Neutropenia-monocytopenia-deafness syndrome
- Neutropenia, lethal congenital, with eosinophilia
- Nevus comedonicus syndrome
- Nevus of Ito
- New-onset refractory status epilepticus
- Nicolaides-Baraitser syndrome
- Niemann-Pick disease, type A
- Niemann-Pick disease, type B
- Niemann-Pick disease, type C
- Niemann-Pick disease, type C2
- Night blindness-skeletal anomalies-dysmorphism syndrome
- Nijmegen breakage syndrome-like disorder
- NIK deficiency
- Nipah virus disease
- Nocardiosis
- Nodular neuronal heterotopia
- Nodular non-suppurative panniculitis
- Nodular regenerative hyperplasia of the liver
- Non-24-hour sleep-wake syndrome
- Non-acquired combined pituitary hormone deficiency
- Non-acquired combined pituitary hormone deficiency with spine abnormalities
- Non-amyloid fibrillary glomerulopathy
- Non-distal monosomy 10q
- Non-distal monosomy 12q
- Non-distal trisomy 10q
- Non-distal trisomy 13q
- Non-distal trisomy 9q
- Non-eruption of teeth-maxillary hypoplasia-genu valgum syndrome
- Non-involuting congenital hemangioma
- Non-Langerhans cell histiocytosis
- Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy
- Non-syndromic metopic craniosynostosis
- Nondystrophic myotonia
- Nongerminomatous germ cell tumor
- Nonsyndromic congenital nail disorder 1
- Nonsyndromic congenital nail disorder 2
- Nonsyndromic congenital nail disorder 7
- Noonan syndrome
- Noonan syndrome with multiple lentigines
- Noonan syndrome-like disorder with loose anagen hair
- Normophosphatemic familial tumoral calcinosis
- North Carolina macular dystrophy
- Norum disease
- NPHP3-related Meckel-like syndrome
- NRXN1-related severe neurodevelopmental disorder-motor stereotypies-chronic constipation-sleep-wake cycle disturbance
- Nut midline carcinoma
Find your
condition community
Find Now condition community
Share your
experience with others
Share Now experience with others
Journal your
experience privately
Journal Now experience privately