Disease Browser
Parent Node: Diseases (C) ..Starting node .. Nutritional and Metabolic Diseases (D009750) Child Nodes:
........Metabolic Diseases (D008659) 1434 ........Nutrition Disorders (D009748) 119 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