| Disease Browser
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Parent Node:
 Diseases (C) |
..Starting node
.. Digestive System Diseases (D004066)
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Child Nodes:
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........Biliary Tract Diseases (D001660)  68 |
| ........Digestive System Abnormalities (D004065) 78 |
| ........Digestive System Fistula (D016154) 12 |
| ........Digestive System Neoplasms (D004067) 99 |
| ........Gastrointestinal Diseases (D005767) 357 |
| ........Liver Diseases (D008107) 135 |
| ........Novak syndrome (C537851) |
| ........Pancreatic Diseases (D010182) 51 |
| ........Peritoneal Diseases (D010532) 16 |
Sister Nodes: |
..AARSKOG SYNDROME, AUTOSOMAL DOMINANT (OMIM:100050)
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..ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE (OMIM:201250)
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..Animal Diseases (D000820) 139
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..AORTIC VALVE DISEASE 1 (OMIM:109730)
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..ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS (OMIM:108900)
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..AXENFELD-RIEGER SYNDROME, TYPE 1 (OMIM:180500)
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..AXENFELD-RIEGER SYNDROME, TYPE 2 (OMIM:601499)
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..AXENFELD-RIEGER SYNDROME, TYPE 3 (OMIM:602482)
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..Bacterial Infections and Mycoses (D001423) 620
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..BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA (OMIM:251290)
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..BRACHYDACTYLY, TYPE E1 (OMIM:113300)
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..BRACHYDACTYLY-MENTAL RETARDATION SYNDROME (OMIM:600430)
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..CAPILLARY MALFORMATIONS, CONGENITAL (OMIM:163000)
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..Cardiovascular Diseases (D002318) 1025
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..CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE (OMIM:607706)
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..Chemically-Induced Disorders (D064419) 111
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..CHROMOSOME 13q14 DELETION SYNDROME (OMIM:613884)
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..CHROMOSOME 17p13.1 DELETION SYNDROME (OMIM:613776)
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..CHROMOSOME 8q21.11 DELETION SYNDROME (OMIM:614230)
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..Congenital, Hereditary, and Neonatal Diseases and Abnormalities (D009358) 4904
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..CONOTRUNCAL HEART MALFORMATIONS (OMIM:217095)
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..COUSIN SYNDROME (OMIM:260660)
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..CRANIOECTODERMAL DYSPLASIA 2 (OMIM:613610)
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..CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA (OMIM:219100)
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..D-BIFUNCTIONAL PROTEIN DEFICIENCY (OMIM:261515)
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..DEAFNESS, AUTOSOMAL RECESSIVE 18A (OMIM:602092)
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..DEAFNESS, AUTOSOMAL RECESSIVE 8 (OMIM:601072)
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..Digestive System Diseases (D004066) 640
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..Disorders of Environmental Origin (D007280) 4
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..ECTOPIA LENTIS 1, ISOLATED, AUTOSOMAL DOMINANT (OMIM:129600)
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..ECTOPIA LENTIS 2, ISOLATED, AUTOSOMAL RECESSIVE (OMIM:225100)
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..EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1 (OMIM:601776)
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..Endocrine System Diseases (D004700) 742
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..Eye Diseases (D005128) 1278
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..Female Urogenital Diseases and Pregnancy Complications (D005261) 962
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..FRONTONASAL DYSPLASIA 1 (OMIM:136760)
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..FRONTONASAL DYSPLASIA 2 (OMIM:613451)
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..FRONTONASAL DYSPLASIA 3 (OMIM:613456)
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..GELEOPHYSIC DYSPLASIA 1 (OMIM:231050)
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..GLUT1 DEFICIENCY SYNDROME 2 (OMIM:612126)
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..GOITER, MULTINODULAR 1, WITH OR WITHOUT SERTOLI-LEYDIG CELL TUMORS (OMIM:138800)
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..GREENBERG DYSPLASIA (OMIM:215140)
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..Hemic and Lymphatic Diseases (D006425) 790
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..HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 (OMIM:239300)
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..HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 3 (OMIM:614207)
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..HYPOTRICHOSIS 2 (OMIM:146520)
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..ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11 (OMIM:602400)
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..Immune System Diseases (D007154) 597
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..IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 1 (OMIM:242860)
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..KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT (OMIM:613702)
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..LOEYS-DIETZ SYNDROME 2 (OMIM:610168)
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..Male Urogenital Diseases (D052801) 765
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..MAYER-ROKITANSKY-KUSTER-HAUSER SYNDROME (OMIM:277000)
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..MEGALOBLASTIC ANEMIA 1 (OMIM:261100)
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..MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 1 (OMIM:155600)
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..MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2 (OMIM:155601)
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..MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 3 (OMIM:609048)
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..MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 4 (OMIM:608035)
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..MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 5 (OMIM:613099)
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..MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 7 (OMIM:612263)
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..MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 8 (OMIM:614456)
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..Mental Disorders (D001523) 1080
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..METHYLMALONIC ACIDURIA DUE TO TRANSCOBALAMIN RECEPTOR DEFECT (OMIM:613646)
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..MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE) (OMIM:603041)
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..MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE) (OMIM:613662)
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..MITOCHONDRIAL DNA DEPLETION SYNDROME 6 (HEPATOCEREBRAL TYPE) (OMIM:256810)
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..MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE) (OMIM:271245)
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..MUCOLIPIDOSIS II ALPHA/BETA (OMIM:252500)
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..MUCOLIPIDOSIS III ALPHA/BETA (OMIM:252600)
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..MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE (OMIM:253290)
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..MULTIPLE SYNOSTOSES SYNDROME 1 (OMIM:186500)
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..Musculoskeletal Diseases (D009140) 2320
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..MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO (OMIM:607948)
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..MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, 1 (OMIM:607949)
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..MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, 2 (OMIM:611046)
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..MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, 3 (OMIM:612929)
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..MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, X-LINKED (OMIM:300259)
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..MYOPATHY, SPHEROID BODY (OMIM:182920)
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..Neoplasms (D009369) 1125
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..Nervous System Diseases (D009422) 3641
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..NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A (OMIM:256600)
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..NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B (OMIM:610217)
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..NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A (OMIM:310500)
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..NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B (OMIM:257270)
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..NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C (OMIM:613216)
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..NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A (OMIM:300071)
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..NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR (OMIM:607721)
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..NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA (OMIM:613563)
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..Nutritional and Metabolic Diseases (D009750) 1518
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..Occupational Diseases (D009784) 28
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..Otorhinolaryngologic Diseases (D010038) 602
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..OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA (OMIM:215150)
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..PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL (OMIM:613000)
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..Parasitic Diseases (D010272) 178
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..Pathological Conditions, Signs and Symptoms (D013568) 3149
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..POLYDACTYLY, PREAXIAL II (OMIM:174500)
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..PONTOCEREBELLAR HYPOPLASIA, TYPE 4 (OMIM:225753)
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..PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA (OMIM:113900)
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..PSEUDOHYPOPARATHYROIDISM, TYPE IA (OMIM:103580)
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..RENAL TUBULAR DYSGENESIS (OMIM:267430)
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..Respiratory Tract Diseases (D012140) 422
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..SCAPULOPERONEAL MYOPATHY, MYH7-RELATED (OMIM:181430)
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..SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY (OMIM:613091)
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..Skin and Connective Tissue Diseases (D017437) 1491
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..SPLIT-HAND/FOOT MALFORMATION 2 (OMIM:313350)
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..SPLIT-HAND/FOOT MALFORMATION 3 (OMIM:246560)
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..SPONDYLOCOSTAL DYSOSTOSIS 1, AUTOSOMAL RECESSIVE (OMIM:277300)
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..SPONDYLOCOSTAL DYSOSTOSIS 2, AUTOSOMAL RECESSIVE (OMIM:608681)
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..SPONDYLOCOSTAL DYSOSTOSIS 3, AUTOSOMAL RECESSIVE (OMIM:609813)
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..SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE (OMIM:613686)
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..SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS (OMIM:143095)
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..Stomatognathic Diseases (D009057) 594
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..THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE (OMIM:612304)
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..VAN DER WOUDE SYNDROME 1, MODIFIER OF (OMIM:604547)
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..VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY (OMIM:604772)
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..VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 2 (OMIM:611938)
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..VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 3 (OMIM:614021)
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..Virus Diseases (D014777) 307
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..VISCERAL MYOPATHY (OMIM:155310)
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..WAARDENBURG SYNDROME, TYPE 4A (OMIM:277580)
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..Wounds and Injuries (D014947) 274
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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