Familial Hypertrophic Cardiomyopathy
Familial Hypertrophic Cardiomyopathy
About the Disease
Cardiomyopathy, Familial Hypertrophic, 1, also known as familial hypertrophic cardiomyopathy, is related to cardiomyopathy, familial hypertrophic, 11 and cardiomyopathy, familial hypertrophic, 25. An important gene associated with Cardiomyopathy, Familial Hypertrophic, 1 is MYH7 (Myosin Heavy Chain 7), and among its related pathways/superpathways are Sweet Taste Signaling and Actin Nucleation by ARP-WASP Complex. The drugs Spironolactone and Ranolazine have been mentioned in the context of this disorder. Affiliated tissues include heart, skeletal muscle and brain, and related phenotypes are congestive heart failure and arrhythmia
Common Targets
TFRC | HRAS | MYOZ2 | TNNT2 | MYL2 | RAF1 | SHOC2 | ALPK3 | MAP2K2 | MYH6 | TTN | OPA1 | PTPN11 | KLHL24 | ACTC1 | G3845 | MYH7 | MYBPC3 | SCN5A | SOS1

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Other Diseases
Cystitis, Interstitial | Renal Hypouricemia | Smith-Lemli-Opitz Syndrome | Chordoid Glioma | Birk-Barel Syndrome | Cone Dystrophy | Esophagitis | Hyperhomocysteinemia | Chronic Granulomatous Disease, X-linked | Addison Disease | Primary Cutaneous Amyloidosis | Chylomicron Retention Disease | Lymphedema-distichiasis Syndrome | Desbuquois Syndrome | Agoraphobia | Diffuse Intrinsic Pontine Glioma | Proteasome-associated Autoinflammatory Syndrome 2 | Aldosterone Deficiency | Achondrogenesis | Agnathia-Otocephaly Complex | Vascular Calcification | Lymphoma, B-cell | Blomstrand Osteochondrodysplasia | Myotonic Disorders | Pseudohypoparathyroidism Type 1A | Chondromyxoid Fibroma | Diabetes | Nutrition Disorders | Chronic Inflammatory Demyelinating Polyneuropathy | Fowler's Syndrome | Myasthenia Gravis | Spinal Muscular Atrophy | Bardet-Biedl Syndrome | Methemoglobinemia | Sclerosteosis | Disseminated Intravascular Coagulation | Leukemia-lymphoma, Adult T-cell | 3-M Syndrome | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Diamond-Blackfan Anemia | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Myofibrillar Myopathy | Peeling Skin Syndrome Type B | Autoimmune Disease | Gnathodiaphyseal Dysplasia | Hidradenitis | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Cohen Syndrome | Chylothorax, Congenital | Chiari Malformation Type I | Distal Spinal Muscular Atrophy | Dystrophy, Cone-rod | Microcephaly, Seizures, And Developmental Delay | Postpartum Depression | Pemphigus | Pterygium | Rash | Myosin Storage Myopathy | Primary Hyperoxaluria Type 1 | Hyperlipidemia, Familial Combined | Stroke, Ischemic | Subacute Sclerosing Panencephalitis | Lafora Disease | Cholecystitis | Microcephaly | Adenosine Deaminase 2 Deficiency | Nestor-Guillermo Progeria Syndrome | Erythematotelangiectatic Rosacea | Sjogren Syndrome | Chronic Kidney Disease | Familial Mediterranean Fever | Incontinentia Pigmenti | Fibrillation, Atrial | Hypercalcemia | Cri-du-chat Syndrome | Erysipelas | Astrocytoma, Anaplastic | Congenital Hemolytic Anemia | Necrobiosis Lipoidica | Tinea Versicolor | Arthritis | Pendred Syndrome | Hereditary Pyropoikilocytosis | Protein S Deficiency | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Myopia | Osteogenesis Imperfecta Type I | Porokeratosis | Charcot-Marie-Tooth Disease Type 2E | Benign Familial Infantile Seizures | Familial Retinal Arterial Macroaneurysm | Platelet Disorders | Neovascular Glaucoma | Diverticulitis | Analgesia | Cervicitis | Hypotrichosis | Dermatomyositis | Pycnodysostosis | Hepatorenal Syndrome | Hereditary Hemorrhagic Telangiectasia Type 2 | Nephrosclerosis | Multicystic Renal Dysplasia | Pseudo-pseudohypoparathyroidism | Meningioma | Asthma, Exercise-induced | Rhabdoid Tumor | Spinal And Bulbar Muscular Atrophy | Dermatofibrosarcoma | Facioscapulohumeral Muscular Dystrophy Type 2 | Adrenal Insufficiency | Stargardt Disease | Acute Kidney Injury | Alstrom Syndrome | Coronary Restenosis | Primary Torsion Dystonia | Leukoencephalopathy, Progressive Multifocal | Polymyositis | Cocaine-Related Disorders | Juvenile Polyposis | Klinefelter Syndrome | Parapsoriasis | Spinocerebellar Ataxia Type 1 | Gout | Zellweger Syndrome | Hemolytic Uremic Syndrome | Sarcoma, Endometrial Stromal | Anal Fissure | Spondylocostal Dysostosis | Arrhythmogenic Right Ventricular Cardiomyopathy | Porphyria Cutanea Tarda | Tibial Muscular Dystrophy | Myhre Syndrome | Adult Polyglucosan Body Disease | Carcinoma, Squamous Cell | Carbamoyl Phosphate Synthetase I Deficiency | Spinocerebellar Ataxia Type 42 | Hypogammaglobulinemia | Motor Neuron Diseases | Syncope | TARP Syndrome | Protein C Deficiency | Brugada Syndrome 1 | Disseminated Superficial Actinic Porokeratosis | T-cell Chronic Lymphocytic Leukemia | Liver Diseases | Pituitary Dwarfism | Neurotoxicity | Congenital Mirror Movements | Usher Syndrome Type IIC | Ganglioneuroma | Periventricular Nodular Heterotopia | Bronchitis, Chronic | Pneumonia, Viral | Familial Episodic Pain Syndrome | Hypotension, Orthostatic | Adrenomyeloneuropathy | Restless Legs Syndrome | Primrose Syndrome | Glaucomatocyclitic Crisis | Smith-Magenis Syndrome | Colitis | Hairy Cell Leukemia | Prolactinoma | Omenn Syndrome | Spinocerebellar Ataxia Type 14 | Anxiety Disorders | Genitopatellar Syndrome | Colitis, Microscopic | Familial Hyperaldosteronism | Joubert Syndrome | Retinal Diseases | Liebenberg Syndrome | Sleep Apnea, Obstructive | Multicentric Carpotarsal Osteolysis Syndrome | Cole-Carpenter Syndrome | Fragile X Syndrome | Esotropia | Familial Pheochromocytoma-paraganglioma | LEOPARD Syndrome | Treacher Collins Syndrome | Thalassemia | 3C Syndrome | Enterocolitis, Necrotizing | Gastritis | Thalassemia, Beta | Exostoses | Eosinophilic Asthma | Schizophrenia | Bacterial Meningitis | Alcoholism | Migraine | Schistosomiasis Mansoni | Hyperprolactinemia | Myoclonic Epilepsy With Ragged Red Fibers | Phosphoglycerate Dehydrogenase Deficiency | Preaxial Polydactyly | Lymphoma, Follicular | Speech Disorders | Meier-Gorlin Syndrome | Pulverulent Zonular Cataract | Charcot-Marie-Tooth Disease Type 4E | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Anodontia | Spinocerebellar Ataxia Type 28 | Spinocerebellar Ataxia Type 27 | Babesiosis | Malonyl-CoA Decarboxylase Deficiency | Spondyloarthritis | Rickets | Gardner Syndrome | Vitelliform Macular Dystrophy | Granular Corneal Dystrophy | Osteogenesis Imperfecta Type VI | Charcot-Marie-Tooth Disease Type 2D | Anterior Segment Dysgenesis | Ligneous Conjunctivitis | Thin Basement Membrane Disease | Compartment Syndrome | Acute Motor Axonal Neuropathy | Sleep Apnea, Central | Anorchia | Craniometaphyseal Dysplasia | Myocarditis | Hereditary Spherocytosis | Pityriasis Rubra Pilaris | Connective Tissue Disorders | Spondylo-ocular Syndrome | Spinocerebellar Ataxia Type 5 | Schwannomatosis | Arteriovenous Malformations | Delayed Sleep Phase Syndrome | Primary Lateral Sclerosis | Haim-Munk Syndrome | Myocardial Infarction | Vestibular Disease | Polycythemia Vera | Postpoliomyelitis Syndrome | Joubert Syndrome 2 | Crigler-Najjar Syndrome | Viral Meningitis | Galactosialidosis | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Blepharitis | Panniculitis | Nephrotic Syndrome | Dysfibrinogenemia | Reye Syndrome | Primary Hyperoxaluria | Keratoconus | Hyperparathyroidism, Primary | Angelman Syndrome | Non-Langerhans Cell Histiocytosis | POEMS Syndrome | Budd-Chiari Syndrome | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Pupil Disorders | Alkaptonuria | Endometritis | Dementia | Retinal Dystrophy, Early-onset Severe | Dementia, Vascular | Nemaline Myopathy | Fibromyalgia | Stiff-man Syndrome | ACTH-independent Macronodular Adrenal Hyperplasia | Idiopathic Pulmonary Fibrosis | Schizoaffective Disorder | Extramammary Paget's Disease | Pseudoexfoliation Syndrome | Hypermethioninemia | Gerodermia Osteodysplastica | Pleomorphic 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Type 8 | Absence Epilepsy | Oculocutaneous Albinism Type 4 | Focal Segmental Glomerulosclerosis | Renal Hypomagnesemia 3 | Cardiomyopathy, Dilated, 1L | Neurofibroma, Plexiform | Language Disorders | Borderline Personality Disorder