Disease Browser
Parent Node: Diseases (C) ..Starting node .. Nervous System Diseases (D009422) Child Nodes:
........Alpha-Methylacyl-CoA Racemase Deficiency (C565768) ........Autoimmune Diseases of the Nervous System (D020274) 60 ........Autonomic Nervous System Diseases (D001342) 51 ........Central Nervous System Diseases (D002493) 1489 ........Chronobiology Disorders (D021081) 5 ........Congenital Cataracts, Facial Dysmorphism, And Neuropathy (C565822) ........Cranial Nerve Diseases (D003389) 238 ........Demyelinating Diseases (D003711) 75 ........Marcus Gunn phenomenon (C535908) ........Nervous System Malformations (D009421) 567 ........Nervous System Neoplasms (D009423) 89 ........Neurocutaneous Syndromes (D020752) 42 ........Neurodegenerative Diseases (D019636) 704 ........Neurologic Disease, Infantile Multisystem, with Osseous Fragility (C564954) ........Neurologic Manifestations (D009461) 1586 ........Neuromuscular Diseases (D009468) 811 ........Neuronal intestinal pseudoobstruction (C537394) ........Neurotoxicity Syndromes (D020258) 20 ........Norrie disease (C537849) ........Polyglucosan Body Disease, Adult Form (C564878) ........Restless Legs Syndrome (D012148) 2 ........Roy Maroteaux Kremp syndrome (C535875) ........Sleep Disorders (D012893) 41 ........Tang Hsi Ryu syndrome (C536897) ........Trauma, Nervous System (D020196) 73 ........Trifunctional Protein Deficiency With Myopathy And Neuropathy (C566945) Sister Nodes: ..AARSKOG SYNDROME, AUTOSOMAL DOMINANT (OMIM:100050) ..ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE (OMIM:201250) ..Animal Diseases (D000820) 139 ..AORTIC VALVE DISEASE 1 (OMIM:109730) ..ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS (OMIM:108900) ..AXENFELD-RIEGER SYNDROME, TYPE 1 (OMIM:180500) ..AXENFELD-RIEGER SYNDROME, TYPE 2 (OMIM:601499) ..AXENFELD-RIEGER SYNDROME, TYPE 3 (OMIM:602482) ..Bacterial Infections and Mycoses (D001423) 620 ..BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA (OMIM:251290) ..BRACHYDACTYLY, TYPE E1 (OMIM:113300) ..BRACHYDACTYLY-MENTAL RETARDATION SYNDROME (OMIM:600430) ..CAPILLARY MALFORMATIONS, CONGENITAL (OMIM:163000) ..Cardiovascular Diseases (D002318) 1025 ..CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE (OMIM:607706) ..Chemically-Induced Disorders (D064419) 111 ..CHROMOSOME 13q14 DELETION SYNDROME (OMIM:613884) ..CHROMOSOME 17p13.1 DELETION SYNDROME (OMIM:613776) ..CHROMOSOME 8q21.11 DELETION SYNDROME (OMIM:614230) ..Congenital, Hereditary, and Neonatal Diseases and Abnormalities (D009358) 4904 ..CONOTRUNCAL HEART MALFORMATIONS (OMIM:217095) ..COUSIN SYNDROME (OMIM:260660) ..CRANIOECTODERMAL DYSPLASIA 2 (OMIM:613610) ..CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA (OMIM:219100) ..D-BIFUNCTIONAL PROTEIN DEFICIENCY (OMIM:261515) ..DEAFNESS, AUTOSOMAL RECESSIVE 18A (OMIM:602092) ..DEAFNESS, AUTOSOMAL RECESSIVE 8 (OMIM:601072) ..Digestive System Diseases (D004066) 640 ..Disorders of Environmental Origin (D007280) 4 ..ECTOPIA LENTIS 1, ISOLATED, AUTOSOMAL DOMINANT (OMIM:129600) ..ECTOPIA LENTIS 2, ISOLATED, AUTOSOMAL RECESSIVE (OMIM:225100) ..EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1 (OMIM:601776) ..Endocrine System Diseases (D004700) 742 ..Eye Diseases (D005128) 1278 ..Female Urogenital Diseases and Pregnancy Complications (D005261) 962 ..FRONTONASAL DYSPLASIA 1 (OMIM:136760) ..FRONTONASAL DYSPLASIA 2 (OMIM:613451) ..FRONTONASAL DYSPLASIA 3 (OMIM:613456) ..GELEOPHYSIC DYSPLASIA 1 (OMIM:231050) ..GLUT1 DEFICIENCY SYNDROME 2 (OMIM:612126) ..GOITER, MULTINODULAR 1, WITH OR WITHOUT SERTOLI-LEYDIG CELL TUMORS (OMIM:138800) ..GREENBERG DYSPLASIA (OMIM:215140) ..Hemic and Lymphatic Diseases (D006425) 790 ..HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 (OMIM:239300) ..HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 3 (OMIM:614207) ..HYPOTRICHOSIS 2 (OMIM:146520) ..ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11 (OMIM:602400) ..Immune System Diseases (D007154) 597 ..IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 1 (OMIM:242860) ..KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT (OMIM:613702) ..LOEYS-DIETZ SYNDROME 2 (OMIM:610168) ..Male Urogenital Diseases (D052801) 765 ..MAYER-ROKITANSKY-KUSTER-HAUSER SYNDROME (OMIM:277000) ..MEGALOBLASTIC ANEMIA 1 (OMIM:261100) ..MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 1 (OMIM:155600) ..MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2 (OMIM:155601) ..MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 3 (OMIM:609048) ..MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 4 (OMIM:608035) ..MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 5 (OMIM:613099) ..MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 7 (OMIM:612263) ..MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 8 (OMIM:614456) ..Mental Disorders (D001523) 1080 ..METHYLMALONIC ACIDURIA DUE TO TRANSCOBALAMIN RECEPTOR DEFECT (OMIM:613646) ..MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE) (OMIM:603041) ..MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE) (OMIM:613662) ..MITOCHONDRIAL DNA DEPLETION SYNDROME 6 (HEPATOCEREBRAL TYPE) (OMIM:256810) ..MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE) (OMIM:271245) ..MUCOLIPIDOSIS II ALPHA/BETA (OMIM:252500) ..MUCOLIPIDOSIS III ALPHA/BETA (OMIM:252600) ..MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE (OMIM:253290) ..MULTIPLE SYNOSTOSES SYNDROME 1 (OMIM:186500) ..Musculoskeletal Diseases (D009140) 2320 ..MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO (OMIM:607948) ..MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, 1 (OMIM:607949) ..MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, 2 (OMIM:611046) ..MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, 3 (OMIM:612929) ..MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, X-LINKED (OMIM:300259) ..MYOPATHY, SPHEROID BODY (OMIM:182920) ..Neoplasms (D009369) 1125 ..Nervous System Diseases (D009422) 3641 ..NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A (OMIM:256600) ..NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B (OMIM:610217) ..NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A (OMIM:310500) ..NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B (OMIM:257270) ..NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C (OMIM:613216) ..NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A (OMIM:300071) ..NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR (OMIM:607721) ..NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA (OMIM:613563) ..Nutritional and Metabolic Diseases (D009750) 1518 ..Occupational Diseases (D009784) 28 ..Otorhinolaryngologic Diseases (D010038) 602 ..OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA (OMIM:215150) ..PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL (OMIM:613000) ..Parasitic Diseases (D010272) 178 ..Pathological Conditions, Signs and Symptoms (D013568) 3149 ..POLYDACTYLY, PREAXIAL II (OMIM:174500) ..PONTOCEREBELLAR HYPOPLASIA, TYPE 4 (OMIM:225753) ..PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA (OMIM:113900) ..PSEUDOHYPOPARATHYROIDISM, TYPE IA (OMIM:103580) ..RENAL TUBULAR DYSGENESIS (OMIM:267430) ..Respiratory Tract Diseases (D012140) 422 ..SCAPULOPERONEAL MYOPATHY, MYH7-RELATED (OMIM:181430) ..SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY (OMIM:613091) ..Skin and Connective Tissue Diseases (D017437) 1491 ..SPLIT-HAND/FOOT MALFORMATION 2 (OMIM:313350) ..SPLIT-HAND/FOOT MALFORMATION 3 (OMIM:246560) ..SPONDYLOCOSTAL DYSOSTOSIS 1, AUTOSOMAL RECESSIVE (OMIM:277300) ..SPONDYLOCOSTAL DYSOSTOSIS 2, AUTOSOMAL RECESSIVE (OMIM:608681) ..SPONDYLOCOSTAL DYSOSTOSIS 3, AUTOSOMAL RECESSIVE (OMIM:609813) ..SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE (OMIM:613686) ..SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS (OMIM:143095) ..Stomatognathic Diseases (D009057) 594 ..THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE (OMIM:612304) ..VAN DER WOUDE SYNDROME 1, MODIFIER OF (OMIM:604547) ..VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY (OMIM:604772) ..VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 2 (OMIM:611938) ..VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 3 (OMIM:614021) ..Virus Diseases (D014777) 307 ..VISCERAL MYOPATHY (OMIM:155310) ..WAARDENBURG SYNDROME, TYPE 4A (OMIM:277580) ..Wounds and Injuries (D014947) 274 Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM , CTD