Disease

Macrophagic Myofasciitis

About the Disease
Macrophagic Myofasciitis, also known as mmf, is related to mycophenolate mofetil embryopathy and myopathy. Affiliated tissues include skeletal muscle, brain and breast, and related phenotypes are fatigue and fever

Common Targets
ATG2A | ULK2 | ATG10 | MAP1LC3A

疾病靶点研报
Macrophagic Myofasciitis

Note: If you'd like to get a target analysis report for Macrophagic Myofasciitis, or if you are interested to learn how our AI-powered BDE-Chem can design therapeutic molecules to interact with the target(s) above against the disease of Macrophagic Myofasciitis at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Myocardial Infarction | Arteriovenous Malformations | Ollier Disease | Blue Nevus | Anterior Segment Dysgenesis | Periventricular Nodular Heterotopia | Desmosterolosis | Spasticity | Orthostatic Intolerance | Kashin-Beck Disease | Pachyonychia Congenita | Danon Disease | Miyoshi Myopathy | Melnick-Needles Syndrome | Fragile X Syndrome | Chronic Neutrophilic Leukemia | Ataxia-ocular Apraxia 2 | Benign Familial Infantile Seizures | Gliosarcoma | Acrodysostosis | Familial Glucocorticoid Deficiency | Neurofibromatosis | Basal Ganglia Disease | Adrenomyeloneuropathy | Hypothyroidism | Pulmonary Alveolar Microlithiasis | Episodic Ataxia | Feingold Syndrome | Stargardt Disease | Melanocytic Nevus | Gastritis, Atrophic | Hemoglobinopathies | Myelomeningocele | Lymphoma, Primary Cutaneous Anaplastic Large Cell | KBG Syndrome | Blastomycosis | Xeroderma Pigmentosum Variant Type | Familial Exudative Vitreoretinopathy | Sengers Syndrome | Familial Dysautonomia | Narcolepsy | Pituitary Stalk Interruption Syndrome | Chromosome 9q34.3 Deletion Syndrome | Neutrophilia | Seizures-scoliosis-macrocephaly Syndrome | Frontotemporal Dementia | Diabetes Type 1 | Joubert Syndrome 2 | Prolactinoma | Harlequin Ichthyosis | Angelman Syndrome | Atherosclerosis | Stromal Corneal Dystrophy | Spinocerebellar Ataxia Type 13 | Gastritis | Epithelioid Hemangioma | Epidermolysis Bullosa Dystrophica | Chronic Leukemia | Robinow Syndrome | Addison Disease | Immunoproliferative Disorders | Monilethrix | Hypospadias | Hemophagocytic Lymphohistiocytosis | Hypogammaglobulinemia | Cavitary Optic Disc Anomalies | Discoid Lupus Erythematosus | Focal Facial Dermal Dysplasia | Spinocerebellar Ataxia Type 27 | Craniolenticulosutural Dysplasia | Plasmacytoma | Retinoblastoma | Gestational Trophoblastic Disease | Hypertelorism | Glioblastoma | Angiosarcoma | Hyperbilirubinemia, Neonatal | Glycogen Storage Disease Type 1a | Histoplasmosis | Turner's Syndrome | Multiple Hamartoma Syndrome | MIRAGE Syndrome | Cholera | Macular Corneal Dystrophy | Osteoporosis-pseudoglioma Syndrome | Early Infantile Epileptic Encephalopathy | DiGeorge Syndrome | Sclerosteosis | Spinocerebellar Ataxia Type 20 | Perry Syndrome | Waardenburg Syndrome | Endometriosis | NDH Syndrome | Uremia | GLUT1 Deficiency Syndrome | Persistent Fetal Circulation | Phenylketonuria II | Acanthosis Nigricans | Osteochondroma | Neurodegeneration With Brain Iron Accumulation | Parkinson's Disease | Porphyria, Acute Intermittent | Congenital Heart Block | Acute Lymphocytic Leukemia | Eclampsia | Follicular Dendritic Cell Sarcoma | Blastoma, Pleuropulmonary | Priapism | Primary Ovarian Insufficiency | Mixed Connective Tissue Disease | Malignant Peripheral Nerve Sheath Tumor | Dyskeratosis Congenita | Angiomyolipoma | Dystrophy, Cone-rod | GNE Myopathy | Cystinosis | AIDS Dementia Complex | Blepharo-cheilo-odontic Syndrome | Hyperkeratosis | Lymphangiomatosis | Adenomyosis | Pseudoexfoliation Syndrome | Myofibromatosis | Down Syndrome | Hartnup Disease | Keratosis, Actinic | Hypersomnia | Warsaw Breakage Syndrome | Craniofrontonasal Syndrome | Primary Familial Brain Calcification | Adenylosuccinate Lyase Deficiency | Subacute Sclerosing Panencephalitis | Sarcosinemia | Liver Failure | Major Depression | Hypobetalipoproteinemias | Pontocerebellar Hypoplasia Type 7 | Keratitis-ichthyosis-deafness Syndrome | Hereditary Spastic Paraplegia | Trichotillomania | Insulin Resistance | Silver-Russell Syndrome | Tremor | Huntington's Disease | Macular Corneal Dystrophy Type 1 | Adult Polyglucosan Body Disease | Alstrom Syndrome | Esophagitis | Carcinoma, Merkel Cell | Erythematotelangiectatic Rosacea | Hypolipoproteinemia | Congenital Heart Defects | Johanson-Blizzard Syndrome | Graft-versus-host Disease | Ocular Hypertension | Influenza | Reflex Epilepsy | Alzheimer Disease, Late Onset | Congenital Adrenal Hyperplasia 1 | Porencephaly | Obesity | Cohen Syndrome | Carney-Stratakis Syndrome | Autosomal Recessive Spastic Paraplegia Type 35 | Hypopituitarism | Van Der Knaap Disease | Retinal Dystrophy, Early-onset Severe | Heart Septal Defects | Lymphangioleiomyomatosis | Uterine Leiomyoma | Hypotrichosis | Familial Retinal Arterial Macroaneurysm | Usher Syndrome Type II | Glycogen Storage Disease Type 5 | Encephalitis, Tick-borne | Hereditary Hemorrhagic Telangiectasia Type 2 | Exotropia | Anorchia | Hydronephrosis | Familial Isolated Hyperparathyroidism | Heterotopic Ossification | Hypercalciuria | Pemphigus Foliaceus | Meningitis | Osteoporosis, Postmenopausal | Thrombophilia | Dominant Optic Atrophy | CHOPS Syndrome | Richter's Syndrome | Polyradiculopathy | Oral Lichen Planus | Saul-Wilson Syndrome | Amenorrhea | Unverricht-Lundborg Syndrome | Aromatic L-amino Acid Decarboxylase Deficiency | Combined Deficiency Of Factor V And Factor VIII | Seborrheic Dermatitis | Acne Vulgaris | LMNA-related Congenital Muscular Dystrophy | Nijmegen Breakage Syndrome | Nasodigitoacoustic Syndrome | Glutaric Aciduria Type 3 | Chiari Malformation Type I | Dysgerminoma | Bone Giant Cell Tumor | Hyperinsulinemia | Aarskog-Scott Syndrome | Vulvovaginitis | Osteopathia Striata With Cranial Sclerosis | Osteonecrosis Of The Jaw | Liver Diseases | Ectopia Lentis, Isolated, Autosomal Recessive | Intestinal Obstruction | Swine Influenza | Arthritis, Reactive | Klinefelter Syndrome | Exostoses | Congestive Heart Failure | Poirier-Bienvenu Neurodevelopmental Syndrome | Neurofibroma | Primary Erythromelalgia | Thin Basement Membrane Disease | Hypoplastic Left Heart Syndrome | Dystonia-parkinsonism, X-linked | N-acetylglutamate Synthase Deficiency | Triple A Syndrome | Nephrotic Syndrome | DEND Syndrome | Conduct Disorder | Lung Diseases | Anorectal Malformations | Acute Myeloid Leukemia | 3-methylglutaconic Aciduria Type IV | Tibial Muscular Dystrophy | Meningioma | Pycnodysostosis | Fibromyalgia | Pneumococcal Meningitis | Infantile Neuroaxonal Dystrophy | Heterotaxy | Corneal Ulcer | Neuroma | Hepatorenal Syndrome | T-cell Leukemia | Basal Ganglia Cerebrovascular Disease | Tic Disorder | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Bethlem Myopathy | Coronary Heart Disease | Takayasu's Arteritis | Pseudohypoparathyroidism Type 1A | Sarcoidosis | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Nephropathy | Cholecystitis | Tyrosinemia Type 2 | Trachoma | C3 Glomerulopathy | Cornelia De Lange Syndrome | Lewy Body Dementia | Congenital Mirror Movements | Vitamin K Deficiency | Fraser Syndrome | Pyloric Stenosis, Infantile Hypertrophic | Duane Retraction Syndrome | Bulimia Nervosa | Focal Segmental Glomerulosclerosis | Diabetes Insipidus, Neurogenic | VEXAS Syndrome | Polycystic Kidney, Autosomal Recessive | Impulse Control Disorder | COACH Syndrome | Calcium Pyrophosphate Deposition Disease | Retinopathy Of Prematurity | Thyroid Hormone Resistance | Pyruvate Decarboxylase Deficiency | Isobutyryl-CoA Dehydrogenase Deficiency | Autosomal Recessive Spastic Paraplegia Type 75 | Polymyositis | Biotinidase Deficiency | Dystonia | Charcot-Marie-Tooth Disease | Camptocormia | Hepatic Steatosis | Leukodystrophies | Communication Disorders | Megalencephaly | Hyperlipidemia Type V | Hemorrhagic Disorders | Chronic Kidney Disease | Usher Syndrome | Retinoschisis | Zimmermann-Laband Syndrome | Superficial Spreading Melanoma | Keratocystic Odontogenic Tumor | Hydrolethalus Syndrome | Periventricular Leukomalacia | Erdheim-Chester Disease | Graves Disease | Optic Nerve Hypoplasia, Bilateral | Mitochondrial DNA Depletion Syndrome | Pseudoachondroplasia | Actinomycetoma | Familial Mediterranean Fever | Mastitis | Pseudohypoaldosteronism | Bone Marrow Necrosis | X-linked Charcot-Marie-Tooth Disease | Pityriasis Rubra Pilaris | Silicosis | Postpoliomyelitis Syndrome | Malnutrition | Gout | Primary Torsion Dystonia | Hypertension | Pyruvate Carboxylase Deficiency Disease | Hyperinsulinism-hyperammonemia Syndrome | Nephrotic Syndrome Type 1 | Galloway-Mowat Syndrome | Mast Cell Leukemia | Acrocallosal Syndrome | Maple Syrup Urine Disease | Periodic Limb Movement Disorder | Benign Familial Pemphigus | Charcot-Marie-Tooth Disease Type 2D | Pheochromocytoma | Optic Neuritis | Myocarditis | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Congenital Nephrotic Syndrome | Goldenhar Syndrome | Schamberg Disease | Genitopatellar Syndrome | Lupus Erythematosus | Conn Syndrome | Relapsing Polychondritis | Filariasis | IgA Nephropathy | T-cell Lymphoma, Subcutaneous Panniculitis-like | Neural Tube Defect | Sotos Syndrome | Mood Disorder | Pancreatitis, Chronic | Cancer, Prostate | Schnyder Crystalline Corneal Dystrophy | Neuroendocrine Cancer | Still Disease | Tetanus | Neurodevelopmental Disorders | Parapsoriasis | Meleda Disease | Wolfram Syndrome 2 | Bartsocas-Papas Syndrome | Hepatitis D | Papillon-Lefevre Syndrome | Protein S Deficiency | Primary Cutaneous Amyloidosis | Astrocytoma, Anaplastic | Osteitis | Epidermolysis Bullosa Simplex, Generalized | Acute Generalized Exanthematous Pustulosis | Antithrombin III Deficiency | Kaposiform Hemangioendothelioma | Rothmund-Thomson Syndrome | VACTERL/VATER Association | Anorexia Nervosa | Fukuyama Congenital Muscular Dystrophy | Multifocal Motor Neuropathy | Schizophrenia | Acute Lung Injury | Xeroderma Pigmentosum | Nutrition Disorders | Progressive Familial Intrahepatic Cholestasis | Osteogenesis Imperfecta Type II | Hepatitis, Chronic | Corneal Dystrophy | Malignant Fibrous Histiocytoma | Synovitis | Oculopharyngeal Muscular Dystrophy | 3-hydroxy-3-methylglutaric Aciduria | Thrombophlebitis | Leiomyoma | Multiple Sclerosis, Secondary Progressive | Recurrent Respiratory Papillomatosis | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Opisthorchiasis | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | WAGR Syndrome | Senior-Loken Syndrome | Cholangitis | Bursitis | Focal Cortical Dysplasia Type 2 | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Arthrogryposis | Proximal Symphalangism | Hypoproteinemia, Hypercatabolic | Retinal Detachment | Prostatitis | Blue Rubber Bleb Nevus Syndrome