| Disease Name |
Symbol |
Acronym |
| N-Acetylaspartate Deficiency
|
NCT013
|
|
| N-Acetylglutamate Synthase Deficiency
|
NCT003
|
|
| Nablus Mask-Like Facial Syndrome
|
NBL001
|
|
| Naegeli-Franceschetti-Jadassohn Syndrome
|
NGL001
|
|
| Nail Disease
|
NLD001
|
|
| Nail Disorder, Nonsyndromic Congenital, 1
|
NLD009
|
|
| Nail Disorder, Nonsyndromic Congenital, 10
|
NLD016
|
|
| Nail Disorder, Nonsyndromic Congenital, 3
|
NLD012
|
|
| Nail Disorder, Nonsyndromic Congenital, 4
|
NLD014
|
|
| Nail Disorder, Nonsyndromic Congenital, 8
|
NLD015
|
|
| Nail Disorder, Nonsyndromic Congenital, 9
|
NLD006
|
|
| Nail Dysplasia, Isolated Congenital
|
NLD003
|
|
| Nail-Patella Syndrome
|
NLP001
|
|
| Nakajo Syndrome
|
NKJ001
|
|
| Nance-Horan Syndrome
|
NNC002
|
|
| Nanophthalmos 1
|
NNP017
|
|
| Nanophthalmos 2
|
NNP011
|
|
| Nanophthalmos 3
|
NNP008
|
|
| Nanophthalmos 4
|
NNP012
|
|
| Narcissistic Personality Disorder
|
NRC003
|
|
| Narcolepsy
|
NRC002
|
|
| Narcolepsy 1
|
NRC009
|
|
| Narcolepsy 2
|
NRC010
|
|
| Narcolepsy 3
|
NRC011
|
|
| Narcolepsy 4
|
NRC012
|
|
| Narcolepsy 5
|
NRC013
|
|
| Narcolepsy 6
|
NRC018
|
|
| Narcolepsy 7
|
NRC017
|
|
| Nasal Cavity Adenocarcinoma
|
NSL003
|
|
| Nasal Cavity Cancer
|
NSL008
|
|
| Nasal Cavity Disease
|
NSL022
|
|
| Nasal Cavity Lymphoma
|
NSL004
|
|
| Nasal Cavity Squamous Cell Carcinoma
|
NSL006
|
|
| Nasopalpebral Lipoma-Coloboma Syndrome
|
NSP016
|
|
| Nasopharyngeal Carcinoma
|
NSP012
|
|
| Nasopharyngeal Carcinoma 2
|
NSP009
|
|
| Nasopharyngeal Carcinoma 3
|
NSP015
|
|
| Nasopharyngeal Disease
|
NSP003
|
|
| Nasopharyngitis
|
NSP002
|
|
| Native American Myopathy
|
NTV001
|
|
| Natowicz Syndrome
|
NTW001
|
|
| Natural Killer Cell Leukemia
|
NTR003
|
|
| Naxos Disease
|
NXS001
|
|
| Nebulin-Related Early-Onset Distal Myopathy
|
NBL003
|
|
| Necatoriasis
|
NCT001
|
|
| Necrobiosis Lipoidica
|
NCR002
|
|
| Necrobiotic Xanthogranuloma
|
NCR009
|
|
| Necrotizing Fasciitis
|
NCR007
|
|
| Necrotizing Gastritis
|
NCR005
|
|
| Necrotizing Sialometaplasia
|
NCR003
|
|
| Necrotizing Soft Tissue Infection
|
NCR014
|
|
| Necrotizing Ulcerative Gingivitis
|
NCR001
|
|
| Neisseria Meningitidis Infection
|
NSS002
|
|
| Nelson Syndrome
|
NLS001
|
|
| Nemaline Myopathy
|
NML001
|
|
| Nemaline Myopathy 1
|
NML002
|
|
| Nemaline Myopathy 10
|
NML022
|
|
| Nemaline Myopathy 11, Autosomal Recessive
|
NML024
|
|
| Nemaline Myopathy 2
|
NML003
|
|
| Nemaline Myopathy 3
|
NML004
|
|
| Nemaline Myopathy 4
|
NML005
|
|
| Nemaline Myopathy 5
|
NML006
|
|
| Nemaline Myopathy 6
|
NML007
|
|
| Nemaline Myopathy 7
|
NML010
|
|
| Nemaline Myopathy 8
|
NML025
|
|
| Nemaline Myopathy 9
|
NML021
|
|
| Neonatal Abstinence Syndrome
|
NNT008
|
|
| Neonatal Adrenoleukodystrophy
|
NNT017
|
|
| Neonatal Alloimmune Neutropenia
|
NNT054
|
|
| Neonatal Anemia
|
NNT011
|
|
| Neonatal Candidiasis
|
NNT005
|
|
| Neonatal Diabetes Mellitus
|
NNT009
|
|
| Neonatal Glycine Encephalopathy
|
NNT038
|
|
| Neonatal Herpes
|
NNT018
|
|
| Neonatal Hypothyroidism
|
NNT019
|
|
| Neonatal Hypoxic and Ischemic Brain Injury
|
NNT033
|
|
| Neonatal Inflammatory Skin and Bowel Disease
|
NNT037
|
|
| Neonatal Jaundice
|
NNT012
|
|
| Neonatal Leukemia
|
NNT007
|
|
| Neonatal Lupus Erythematosus
|
NNT042
|
|
| Neonatal Marfan Syndrome
|
NNT039
|
|
| Neonatal Meningitis
|
NNT021
|
|
| Neonatal Myasthenia Gravis
|
NNT006
|
|
| Neonatal Period Electroclinical Syndrome
|
NNT041
|
|
| Neonatal Respiratory Failure
|
NNT004
|
|
| Neonatal Stroke
|
NNT024
|
|
| Neonatal Thyrotoxicosis
|
NNT003
|
|
| Neovascular Glaucoma
|
NVS001
|
|
| Nephrocalcinosis
|
NPH003
|
|
| Nephrogenic Adenofibroma
|
NPH006
|
|
| Nephrogenic Adenoma
|
NPH001
|
|
| Nephrogenic Adenoma of the Urethra
|
NPH008
|
|
| Nephrogenic Adenoma of Urinary Bladder
|
NPH002
|
|
| Nephrogenic Syndrome of Inappropriate Antidiuresis
|
NPH013
|
|
| Nephrogenic Systemic Fibrosis
|
NPH018
|
|
| Nephrolithiasis
|
NPH009
|
|
| Nephrolithiasis, Calcium Oxalate
|
NPH091
|
|
| Nephrolithiasis, Uric Acid
|
NPH078
|
|
| Nephrolithiasis, X-Linked Recessive, with Renal Failure
|
NPH098
|
|
| Nephrolithiasis/osteoporosis, Hypophosphatemic, 1
|
NPH056
|
|
| Nephrolithiasis/osteoporosis, Hypophosphatemic, 2
|
NPH042
|
|
| Nephronophthisis
|
NPH005
|
|
| Nephronophthisis 1
|
NPH019
|
|
| Nephronophthisis 11
|
NPH053
|
|
| Nephronophthisis 12
|
NPH067
|
|
| Nephronophthisis 13
|
NPH065
|
|
| Nephronophthisis 14
|
NPH071
|
|
| Nephronophthisis 15
|
NPH069
|
|
| Nephronophthisis 16
|
NPH068
|
|
| Nephronophthisis 18
|
NPH075
|
|
| Nephronophthisis 19
|
NPH077
|
|
| Nephronophthisis 2
|
NPH030
|
|
| Nephronophthisis 20
|
NPH086
|
|
| Nephronophthisis 3
|
NPH031
|
|
| Nephronophthisis 4
|
NPH032
|
|
| Nephronophthisis 7
|
NPH033
|
|
| Nephronophthisis 9
|
NPH035
|
|
| Nephronophthisis-Like Nephropathy 1
|
NPH037
|
|
| Nephropathy with Pretibial Epidermolysis Bullosa and Deafness
|
NPH014
|
|
| Nephropathy, Progressive, with Deafness
|
NPH050
|
|
| Nephrosclerosis
|
NPH010
|
|
| Nephrotic Syndrome
|
NPH012
|
|
| Nephrotic Syndrome 14
|
NPH094
|
|
| Nephrotic Syndrome 15
|
NPH092
|
|
| Nephrotic Syndrome 16
|
NPH101
|
|
| Nephrotic Syndrome, Idiopathic, Steroid-Resistant
|
NPH026
|
|
| Nephrotic Syndrome, Type 1
|
NPH055
|
|
| Nephrotic Syndrome, Type 10
|
NPH076
|
|
| Nephrotic Syndrome, Type 11
|
NPH095
|
|
| Nephrotic Syndrome, Type 12
|
NPH096
|
|
| Nephrotic Syndrome, Type 13
|
NPH093
|
|
| Nephrotic Syndrome, Type 2
|
NPH049
|
|
| Nephrotic Syndrome, Type 3
|
NPH054
|
|
| Nephrotic Syndrome, Type 4
|
NPH047
|
|
| Nephrotic Syndrome, Type 5, with or Without Ocular Abnormalities
|
NPH039
|
|
| Nephrotic Syndrome, Type 6
|
NPH070
|
|
| Nephrotic Syndrome, Type 7
|
NPH072
|
|
| Nephrotic Syndrome, Type 8
|
NPH073
|
|
| Nephrotic Syndrome, Type 9
|
NPH074
|
|
| Nerve Compression Syndrome
|
NRV004
|
|
| Nerve Growth Factor, Alpha Subunit
|
NRV013
|
|
| Nervous System Cancer
|
NRV006
|
|
| Nervous System Disease
|
NRV007
|
|
| Nestor-Guillermo Progeria Syndrome
|
NST002
|
|
| Netherton Syndrome
|
NTH001
|
|
| Neu-Laxova Syndrome 1
|
NLX004
|
|
| Neu-Laxova Syndrome 2
|
NLX003
|
|
| Neural Crest Tumor
|
NRL008
|
|
| Neural Tube Defects
|
NRL016
|
|
| Neural Tube Defects, Folate-Sensitive
|
NRL018
|
|
| Neuraminidase Deficiency
|
NRM019
|
|
| Neurenteric Cyst
|
NRN022
|
|
| Neurilemmoma
|
NRL005
|
|
| Neurilemmomatosis
|
NRL002
|
|
| Neuritis
|
NRT004
|
|
| Neuroaxonal Dystrophy
|
NRX001
|
|
| Neuroblastoma
|
NRB001
|
|
| Neuroblastoma 2
|
NRB015
|
|
| Neuroblastoma 3
|
NRB014
|
|
| Neuroblastoma 4
|
NRB011
|
|
| Neuroblastoma 5
|
NRB012
|
|
| Neuroblastoma 6
|
NRB013
|
|
| Neuroblastoma 7
|
NRB016
|
|
| Neurodegeneration Due to Cerebral Folate Transport Deficiency
|
NRD004
|
|
| Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy, Childhood-Onset
|
NRD027
|
|
| Neurodegeneration with Brain Iron Accumulation
|
NRD007
|
|
| Neurodegeneration with Brain Iron Accumulation 1
|
NRD017
|
|
| Neurodegeneration with Brain Iron Accumulation 2a
|
NRD033
|
|
| Neurodegeneration with Brain Iron Accumulation 2b
|
NRD009
|
|
| Neurodegeneration with Brain Iron Accumulation 3
|
NRD008
|
|
| Neurodegeneration with Brain Iron Accumulation 4
|
NRD014
|
|
| Neurodegeneration with Brain Iron Accumulation 5
|
NRD032
|
|
| Neurodegeneration with Brain Iron Accumulation 6
|
NRD016
|
|
| Neurodegeneration with Brain Iron Accumulation 7
|
NRD047
|
|
| Neurodegeneration with Brain Iron Accumulation 8
|
NRD048
|
|
| Neurodegeneration, Childhood-Onset, with Brain Atrophy
|
NRD030
|
|
| Neurodermatitis
|
NRD001
|
|
| Neurodevelopmental Disorder with Ataxic Gait, Absent Speech, and Decreased Cortical White Matter
|
NRD040
|
|
| Neurodevelopmental Disorder with Brain, Liver, and Lung Abnormalities
|
NRD050
|
|
| Neurodevelopmental Disorder with Dysmorphic Facies and Distal Limb Anomalies
|
NRD037
|
|
| Neurodevelopmental Disorder with Epilepsy, Cataracts, Feeding Difficulties, and Delayed Brain Myelination
|
NRD031
|
|
| Neurodevelopmental Disorder with Hypotonia, Seizures, and Absent Language
|
NRD023
|
|
| Neurodevelopmental Disorder with Involuntary Movements
|
NRD029
|
|
| Neurodevelopmental Disorder with Microcephaly, Ataxia, and Seizures
|
NRD035
|
|
| Neurodevelopmental Disorder with Microcephaly, Cataracts, and Renal Abnormalities
|
NRD046
|
|
| Neurodevelopmental Disorder with Microcephaly, Epilepsy, and Brain Atrophy
|
NRD042
|
|
| Neurodevelopmental Disorder with Microcephaly, Hypotonia, and Variable Brain Anomalies
|
NRD026
|
|
| Neurodevelopmental Disorder with Microcephaly, Seizures, and Cortical Atrophy
|
NRD038
|
|
| Neurodevelopmental Disorder with Midbrain and Hindbrain Malformations
|
NRD025
|
|
| Neurodevelopmental Disorder with Movement Abnormalities, Abnormal Gait, and Autistic Features
|
NRD044
|
|
| Neurodevelopmental Disorder with or Without Anomalies of the Brain, Eye, or Heart
|
NRD024
|
|
| Neurodevelopmental Disorder with or Without Hyperkinetic Movements and Seizures, Autosomal Dominant
|
NRD034
|
|
| Neurodevelopmental Disorder with or Without Hyperkinetic Movements and Seizures, Autosomal Recessive
|
NRD041
|
|
| Neurodevelopmental Disorder with or Without Seizures and Gait Abnormalities
|
NRD043
|
|
| Neurodevelopmental Disorder with Poor Language and Loss of Hand Skills
|
NRD045
|
|
| Neurodevelopmental Disorder with Progressive Microcephaly, Spasticity, and Brain Anomalies
|
NRD028
|
|
| Neurodevelopmental Disorder with Severe Motor Impairment and Absent Language
|
NRD039
|
|
| Neurodevelopmental Disorder with Spastic Quadriplegia and Brain Abnormalities with or Without Seizures
|
NRD049
|
|
| Neurodevelopmental Disorder-Craniofacial Dysmorphism-Cardiac Defect-Hip Dysplasia Syndrome Due to 9q21 Microdeletion
|
NRD020
|
|
| Neurodevelopmental Disorder, Mitochondrial, with Abnormal Movements and Lactic Acidosis, with or Without Seizures
|
NRD036
|
|
| Neuroendocrine Cell Hyperplasia of Infancy
|
NRN023
|
|
| Neuroendocrine Tumor
|
NRN004
|
|
| Neurofibroma
|
NRF007
|
|
| Neurofibromatosis-Noonan Syndrome
|
NRF008
|
|
| Neurofibromatosis, Familial Spinal
|
NRF016
|
|
| Neurofibromatosis, Type I
|
NRF024
|
|
| Neurofibromatosis, Type Ii
|
NRF023
|
NF2
|
| Neurofibromatosis, Type Iv, of Riccardi
|
NRF026
|
|
| Neurofibrosarcoma
|
NRF003
|
|
| Neurogenic Arthropathy
|
NRG003
|
|
| Neurogenic Bladder
|
NRG002
|
|
| Neurogenic Bowel
|
NRG001
|
|
| Neurogenic Hypertension
|
NRG005
|
|
| Neuroleptic Malignant Syndrome
|
NRL004
|
|
| Neurologic, Endocrine, and Pancreatic Disease, Multisystem, Infantile-Onset
|
NRL023
|
|
| Neuroma
|
NRM004
|
|
| Neuromuscular Disease
|
NRM005
|
|
| Neuromuscular Junction Disease
|
NRM006
|
|
| Neuromyelitis Optica
|
NRM001
|
|
| Neuromyelitis Optica Spectrum Disorder
|
NRM008
|
|
| Neuromyotonia and Axonal Neuropathy, Autosomal Recessive
|
NRM016
|
|
| Neuronal Ceroid Lipofuscinosis
|
NRN021
|
|
| Neuronal Ceroid-Lipofuscinoses
|
NRN005
|
|
| Neuronal Intestinal Dysplasia
|
NRN029
|
|
| Neuronal Intranuclear Inclusion Disease
|
NRN008
|
|
| Neuronal Migration Disorders
|
NRN016
|
|
| Neuronitis
|
NRN002
|
|
| Neuronopathy, Distal Hereditary Motor, Type Iia
|
NRN035
|
|
| Neuronopathy, Distal Hereditary Motor, Type Iib
|
NRN041
|
|
| Neuronopathy, Distal Hereditary Motor, Type Iic
|
NRN018
|
|
| Neuronopathy, Distal Hereditary Motor, Type Iid
|
NRN026
|
|
| Neuronopathy, Distal Hereditary Motor, Type Ix
|
NRN042
|
|
| Neuronopathy, Distal Hereditary Motor, Type Va
|
NRN037
|
|
| Neuronopathy, Distal Hereditary Motor, Type Vb
|
NRN024
|
|
| Neuronopathy, Distal Hereditary Motor, Type Viia
|
NRN025
|
|
| Neuronopathy, Distal Hereditary Motor, Type Viib
|
NRN040
|
|
| Neuronopathy, Distal Hereditary Motor, Type Viii
|
NRN036
|
|
| Neuropathy
|
NRP001
|
|
| Neuropathy with Hearing Impairment
|
NRP028
|
|
| Neuropathy, Ataxia, and Retinitis Pigmentosa
|
NRP045
|
|
| Neuropathy, Congenital Hypomyelinating or Amyelinating, Autosomal Recessive
|
NRP060
|
|
| Neuropathy, Hereditary Motor and Sensory, Okinawa Type
|
NRP009
|
|
| Neuropathy, Hereditary Motor and Sensory, Russe Type
|
NRP010
|
|
| Neuropathy, Hereditary Motor and Sensory, Type Via
|
NRP059
|
|
| Neuropathy, Hereditary Motor and Sensory, Type Vib
|
NRP043
|
|
| Neuropathy, Hereditary Motor and Sensory, with Deafness, Mental Retardation, and Absent Sensory Large Myelinated Fibers
|
NRP046
|
|
| Neuropathy, Hereditary Sensory and Autonomic, Type I, with Cough and Gastroesophageal Reflux
|
NRP049
|
|
| Neuropathy, Hereditary Sensory and Autonomic, Type Ia
|
NRP033
|
|
| Neuropathy, Hereditary Sensory and Autonomic, Type Ic
|
NRP040
|
|
| Neuropathy, Hereditary Sensory and Autonomic, Type Iia
|
NRP053
|
|
| Neuropathy, Hereditary Sensory and Autonomic, Type Iib
|
NRP018
|
|
| Neuropathy, Hereditary Sensory and Autonomic, Type Iii
|
NRP054
|
|
| Neuropathy, Hereditary Sensory and Autonomic, Type V
|
NRP037
|
|
| Neuropathy, Hereditary Sensory and Autonomic, Type Vi
|
NRP038
|
|
| Neuropathy, Hereditary Sensory and Autonomic, Type Vii
|
NRP031
|
|
| Neuropathy, Hereditary Sensory and Autonomic, Type Viii
|
NRP044
|
|
| Neuropathy, Hereditary Sensory, Type Id
|
NRP039
|
|
| Neuropathy, Hereditary Sensory, Type Ie
|
NRP041
|
|
| Neuropathy, Hereditary Sensory, Type if
|
NRP036
|
|
| Neuropathy, Hereditary Sensory, Type Iic
|
NRP029
|
|
| Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive
|
NRP055
|
|
| Neuropathy, Hereditary, with Liability to Pressure Palsies
|
NRP051
|
|
| Neuropathy, Hereditary, with or Without Age-Related Macular Degeneration
|
NRP048
|
|
| Neuropathy, Painful
|
NRP027
|
|
| Neuroretinitis
|
NRR001
|
|
| Neurosarcoidosis
|
NRS005
|
|
| Neuroschistosomiasis
|
NRS001
|
|
| Neurosyphilis
|
NRS003
|
|
| Neurotic Disorder
|
NRT001
|
|
| Neurotic Excoriation
|
NRT002
|
|
| Neurotrophic Keratopathy
|
NRT011
|
|
| Neutral Lipid Storage Disease with Myopathy
|
NTR007
|
|
| Neutropenia
|
NTR004
|
|
| Neutropenia, Nonimmune Chronic Idiopathic, of Adults
|
NTR013
|
|
| Neutropenia, Severe Congenital, 1, Autosomal Dominant
|
NTR047
|
|
| Neutropenia, Severe Congenital, 2, Autosomal Dominant
|
NTR051
|
|
| Neutropenia, Severe Congenital, 3, Autosomal Recessive
|
NTR049
|
|
| Neutropenia, Severe Congenital, 4, Autosomal Recessive
|
NTR050
|
|
| Neutropenia, Severe Congenital, 5, Autosomal Recessive
|
NTR031
|
|
| Neutropenia, Severe Congenital, 6, Autosomal Recessive
|
NTR034
|
|
| Neutropenia, Severe Congenital, 7, Autosomal Recessive
|
NTR044
|
|
| Neutropenia, Severe Congenital, X-Linked
|
NTR036
|
|
| Neutrophil Actin Dysfunction
|
NTR027
|
|
| Neutrophil Immunodeficiency Syndrome
|
NTR006
|
|
| Neutrophil Migration
|
NTR046
|
|
| Neutrophil-Specific Granule Deficiency
|
NTR011
|
|
| Neutrophilia, Hereditary
|
NTR018
|
|
| Neutrophilic Dermatosis, Acute Febrile
|
NTR042
|
|
| Nevus Comedonicus
|
NVS015
|
|
| Nevus of Ota
|
NVS007
|
|
| Nevus, Epidermal
|
NVS017
|
|
| New Daily-Persistent Headache
|
NWD001
|
|
| Newborn Respiratory Distress Syndrome
|
NWB001
|
|
| Newcastle Disease
|
NWC001
|
|
| Newfoundland Rod-Cone Dystrophy
|
NWF001
|
|
| Nicolaides-Baraitser Syndrome
|
NCL006
|
|
| Niemann-Pick Disease
|
NMN002
|
|
| Niemann-Pick Disease Type C, Adult Neurologic Onset
|
NMN011
|
|
| Niemann-Pick Disease Type C, Juvenile Neurologic Onset
|
NMN012
|
|
| Niemann-Pick Disease Type C, Late Infantile Neurologic Onset
|
NMN009
|
|
| Niemann-Pick Disease Type C, Severe Early Infantile Neurologic Onset
|
NMN010
|
|
| Niemann-Pick Disease Type C, Severe Perinatal Form
|
NMN008
|
|
| Niemann-Pick Disease, Type a
|
NMN013
|
|
| Niemann-Pick Disease, Type B
|
NMN016
|
|
| Niemann-Pick Disease, Type C1
|
NMN015
|
|
| Niemann-Pick Disease, Type C2
|
NMN014
|
|
| Night Blindness
|
NGH001
|
|
| Night Blindness, Congenital Stationary, Autosomal Dominant 1
|
NGH021
|
|
| Night Blindness, Congenital Stationary, Autosomal Dominant 2
|
NGH010
|
|
| Night Blindness, Congenital Stationary, Autosomal Dominant 3
|
NGH008
|
|
| Night Blindness, Congenital Stationary, Type 1a
|
NGH026
|
|
| Night Blindness, Congenital Stationary, Type 1b
|
NGH007
|
|
| Night Blindness, Congenital Stationary, Type 1c
|
NGH027
|
|
| Night Blindness, Congenital Stationary, Type 1d
|
NGH028
|
|
| Night Blindness, Congenital Stationary, Type 1e
|
NGH029
|
|
| Night Blindness, Congenital Stationary, Type 1f
|
NGH030
|
|
| Night Blindness, Congenital Stationary, Type 1g
|
NGH022
|
|
| Night Blindness, Congenital Stationary, Type 1h
|
NGH024
|
|
| Night Blindness, Congenital Stationary, Type 2a
|
NGH025
|
|
| Nijmegen Breakage Syndrome
|
NJM001
|
|
| Nijmegen Breakage Syndrome-Like Disorder
|
NJM002
|
|
| Nik Deficiency
|
NKD001
|
|
| Nipples, Supernumerary
|
NPP006
|
|
| Nocardiosis
|
NCR004
|
|
| Nodal Marginal Zone B-Cell Lymphoma
|
NDL020
|
|
| Nodal Marginal Zone Lymphoma
|
NDL024
|
|
| Nodular Basal Cell Carcinoma
|
NDL009
|
|
| Nodular Degeneration of Cornea
|
NDL004
|
|
| Nodular Ganglioneuroblastoma
|
NDL011
|
|
| Nodular Goiter
|
NDL007
|
|
| Nodular Hidradenoma
|
NDL010
|
|
| Nodular Lymphocyte Predominant Hodgkin Lymphoma
|
NDL021
|
|
| Nodular Malignant Melanoma
|
NDL001
|
|
| Nodular Medulloblastoma
|
NDL005
|
|
| Nodular Nonsuppurative Panniculitis
|
NDL003
|
|
| Nodular Prostate
|
NDL006
|
|
| Nodular Regenerative Hyperplasia
|
NDL013
|
|
| Nodular Tenosynovitis
|
NDL002
|
|
| Nodular Urticaria Pigmentosa
|
NDL018
|
|
| Noma
|
NM001
|
|
| Nominal Aphasia
|
NMN001
|
|
| Non-a-E Hepatitis
|
NNH002
|
|
| Non-Classic Congenital Lipoid Adrenal Hyperplasia Due to Star Deficency
|
NNC007
|
|
| Non-Functioning Pancreatic Endocrine Tumor
|
NNF001
|
|
| Non-Functioning Paraganglioma
|
NNF008
|
|
| Non-Functioning Pituitary Adenoma
|
NNF007
|
|
| Non-Gestational Choriocarcinoma
|
NNG001
|
|
| Non-Gestational Ovarian Choriocarcinoma
|
NNG002
|
|
| Non-Hereditary Retinoblastoma
|
NNH011
|
|
| Non-Herpetic Acute Limbic Encephalitis
|
NNH006
|
|
| Non-Invasive Bladder Papillary Urothelial Neoplasm
|
NNN005
|
|
| Non-Langerhans-Cell Histiocytosis
|
NNL001
|
|
| Non-Progressive Predominantly Posterior Cavitating Leukoencephalopathy with Peripheral Neuropathy
|
NNP016
|
|
| Non-Proliferative Fibrocystic Change of the Breast
|
NNP005
|
|
| Non-Secretory Myeloma
|
NNS003
|
|
| Non-Small Cell Lung Cancer, Childhood
|
NNS012
|
|
| Non-Suppurative Otitis Media
|
NNS006
|
|
| Non-Syndromic Genetic Deafness
|
NNS044
|
|
| Non-Syndromic Intellectual Disability
|
NNS031
|
|
| Non-Syndromic Male Infertility Due to Sperm Motility Disorder
|
NNS033
|
|
| Non-Syndromic X-Linked Intellectual Disability
|
NNS032
|
|
| Nonaka Myopathy
|
NNK001
|
|
| Nonalcoholic Fatty Liver Disease
|
NNL004
|
|
| Nonalcoholic Steatohepatitis
|
NNL002
|
|
| Nonarteritic Anterior Ischemic Optic Neuropathy
|
NNR004
|
|
| Nondisjunction
|
NND010
|
|
| Nondystrophic Myotonia
|
NND001
|
|
| Nonphotosensitive Trichothiodystrophy
|
NNP004
|
|
| Nonseminomatous Germ Cell Tumor
|
NNS011
|
|
| Nonspecific Interstitial Pneumonia
|
NNS002
|
|
| Nonsyndromic Deafness
|
NNS007
|
|
| Nonsyndromic Retinitis Pigmentosa
|
NNS043
|
|
| Nontoxic Goiter
|
NNT010
|
|
| Nontuberculous Mycobacterial Lung Disease
|
NNT049
|
|
| Noonan Syndrome 1
|
NNN008
|
|
| Noonan Syndrome 10
|
NNN025
|
|
| Noonan Syndrome 2
|
NNN009
|
|
| Noonan Syndrome 3
|
NNN010
|
|
| Noonan Syndrome 4
|
NNN011
|
|
| Noonan Syndrome 5
|
NNN012
|
|
| Noonan Syndrome 6
|
NNN013
|
|
| Noonan Syndrome 7
|
NNN020
|
|
| Noonan Syndrome 8
|
NNN021
|
|
| Noonan Syndrome 9
|
NNN024
|
|
| Noonan Syndrome with Multiple Lentigines
|
NNN026
|
|
| Noonan Syndrome-Like Disorder with Loose Anagen Hair 1
|
NNN028
|
|
| Noonan Syndrome-Like Disorder with Loose Anagen Hair 2
|
NNN027
|
|
| Noonan Syndrome-Like Disorder with or Without Juvenile Myelomonocytic Leukemia
|
NNN022
|
|
| Noonan-Like/multiple Giant Cell Lesion Syndrome
|
NNN015
|
|
| Normokalemic Periodic Paralysis
|
NRM009
|
|
| Normosmic Congenital Hypogonadotropic Hypogonadism
|
NRM018
|
|
| Norrie Disease
|
NRR002
|
|
| Norse
|
NRS006
|
|
| North American Indian Childhood Cirrhosis
|
NRT006
|
|
| Norwegian Scabies
|
NRW001
|
|
| Nose Disease
|
NSD001
|
|
| Nosophobia
|
NSP004
|
|
| Novelty Seeking Personality Trait
|
NVL002
|
|
| Nsdhl-Related Disorders
|
NSD002
|
|
| Nuclear Senile Cataract
|
NCL001
|
|
| Null Pituitary Adenoma
|
NLL003
|
|
| Null-Cell Leukemia
|
NLL001
|
|
| Nut Allergy
|
NTL004
|
|
| Nut Midline Carcinoma
|
NTM002
|
|
| Nutmeg Liver
|
NTM001
|
|
| Nutritional Deficiency Disease
|
NTR005
|
|
| Nutritional Optic Neuropathy
|
NTR002
|
|
| Nystagmus 1, Congenital, X-Linked
|
NYS017
|
|
| Nystagmus 2, Congenital, Autosomal Dominant
|
NYS003
|
|
| Nystagmus 3, Congenital, Autosomal Dominant
|
NYS004
|
|
| Nystagmus 4, Congenital, Autosomal Dominant
|
NYS005
|
|
| Nystagmus 5, Congenital, X-Linked
|
NYS012
|
|
| Nystagmus 6, Congenital, X-Linked
|
NYS013
|
|
| Nystagmus 7, Congenital, Autosomal Dominant
|
NYS016
|
|
