Familial Isolated Hyperparathyroidism
Familial Isolated Hyperparathyroidism
About the Disease
Hyperparathyroidism 1, also known as familial isolated hyperparathyroidism, is related to hyperparathyroidism 2 with jaw tumors and multiple endocrine neoplasia. An important gene associated with Hyperparathyroidism 1 is CDC73 (Cell Division Cycle 73). The drugs Parathyroid hormone and Cinacalcet have been mentioned in the context of this disorder. Affiliated tissues include kidney, bone and thyroid, and related phenotypes are osteopenia and hypophosphatemia
Common Targets
CASR | CDC73 | LRP5 | FAT3 | TBCE | MEN1 | APC | HDAC4 | TGFB1 | GCM2 | PRKN | G2475 | ITPR2

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Triple A Syndrome | Congenital Dyserythropoietic Anemia Type 1 | Leri Pleonosteosis | Synovitis | Myotonic Disorders | Light Chain Amyloidosis | Liddle Syndrome | Progressive Familial Intrahepatic Cholestasis Type 2 | Hepatorenal Syndrome | Sialoadenitis | Ichthyosis Hystrix, Curth-Macklin Type | Amyloidosis | Otitis Externa | Hepatopulmonary Syndrome | Smith-Lemli-Opitz Syndrome | Spinocerebellar Ataxia Type 2 | Irritable Bowel Syndrome | Borderline Personality Disorder | Sturge-Weber Syndrome | Congenital Ichthyosiform Erythroderma | Cirrhosis | Restless Legs Syndrome | Kernicterus | Castleman Disease | Bruck Syndrome | Dystrophy, Cone-rod | Alopecia Areata | Chronic Inflammatory Demyelinating Polyneuropathy | Hypertensive Nephropathy | Thrombasthenia | Hereditary Inclusion Body Myopathy | Dermatofibrosarcoma | Cocaine-Related Disorders | Acute Chest Syndrome | Cancer, Skin | Neurotoxicity | Dysthymia | Sleep Apnea, Central | Microcephalic Primordial Dwarfism | Chronic Lymphocytic Leukemia | Fukuyama Congenital Muscular Dystrophy | Fahr Disease | Porokeratosis | Pterygium | Gerstmann-Straussler-Scheinker Syndrome | Crimean-Congo Hemorrhagic Fever | 3-M Syndrome | Gliosarcoma | Perivascular Epithelioid Cell Tumor | Corneal Dystrophies, Hereditary | Pulmonary Vein Stenosis | Neurofibromatosis | Myelomeningocele | X-linked Charcot-Marie-Tooth Disease | Cancer, Lung | Thanatophoric Dysplasia | Bronchitis, Chronic | Lymphoma, B-cell | Cousin Syndrome | Toxic Epidermal Necrolysis | Takayasu's Arteritis | Spinocerebellar Ataxia Type 7 | Malaria, Cerebral | Retinal Vasculitis | Aicardi-Goutieres Syndrome | Tinea Versicolor | Nail Disorder, Nonsyndromic Congenital | Hypogammaglobulinemia | Progressive Familial Intrahepatic Cholestasis | Hypotension, Orthostatic | Acute Myeloid Leukemia | Congenital Dysfibrinogenemia | Essential Fructosuria | Trismus-pseudocamptodactyly Syndrome | Scleroderma | Alpha-thalassemia Myelodysplasia Syndrome | Acute Generalized Exanthematous 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