Pulmonary Alveolar Microlithiasis

About the Disease
Pulmonary Alveolar Microlithiasis, also known as pulam, is related to respiratory failure and interstitial lung disease. An important gene associated with Pulmonary Alveolar Microlithiasis is SLC34A2 (Solute Carrier Family 34 Member 2), and among its related pathways/superpathways are Metabolism of proteins and Disease. Affiliated tissues include lung, testes and prostate, and related phenotypes are fatigue and chest pain

Common Targets
CCDC40 | SLC34A2

Note: If you'd like to get a target analysis report for Pulmonary Alveolar Microlithiasis, 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 Pulmonary Alveolar Microlithiasis at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Congenital Afibrinogenemia | Cholelithiasis | Birt-Hogg-Dube Syndrome | Uremic Pruritus | Epilepsy, Generalized | Glycogen Storage Disease Type 3 | Nemaline Myopathy 10 | Chronic Beryllium Disease | ICF Syndrome | Perry Syndrome | Lipid Storage Diseases | Chordoid Glioma | Smith-Lemli-Opitz Syndrome | Retinal Detachment | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Neuromyelitis Optica | Renal Hypomagnesemia 3 | Chronic Granulomatous Disease | Kindler Syndrome | Hepatitis, Chronic | Myhre Syndrome | Chudley-McCullough Syndrome | Cyst | IMAGe Syndrome | Amish Infantile Epilepsy Syndrome | Cerebellofaciodental Syndrome | Retinitis | Early Infantile Epileptic Encephalopathy 1 | Chronic Leukemia | Chondrosarcoma | Spinal Muscular Atrophy Type 2 | Chronic Myeloid Leukemia | Carcinoma In Situ | Hoyeraal-Hreidarsson Syndrome | Swine Influenza | Infertility, Male | Vascular Calcification | Congenital Primary Aphakia | Chediak-Higashi Syndrome | Greenberg Dysplasia | Hamartoma | Renpenning Syndrome | Olmsted Syndrome | Congenital Diaphragmatic Hernia | Myelofibrosis | Histiocytosis | Cholecystitis | Mesothelioma, Malignant | Wolfram Syndrome 2 | Sclerosteosis | Pernicious Anemia | Delirium | Pilomatrix Carcinoma | Epicondylitis | Urolithiasis | Down Syndrome | Spondyloepiphyseal Dysplasia Tarda, X-linked | Acquired Partial Lipodystrophy | Hemoglobinopathies | Prolactinoma | Osteogenesis Imperfecta Type VI | Chronic Kidney Disease | Cryptosporidiosis | C3 Glomerulopathy | Saul-Wilson Syndrome | Arteriovenous Malformations | Multiple Hamartoma Syndrome | Amyloidosis | Astigmatism | Cardiac Sarcoidosis | Anti-NMDA Receptor Encephalitis | Antley-Bixler Syndrome | Gangliosidosis, GM1 | Tracheal Disorders | Peutz-Jeghers Syndrome | Frontometaphyseal Dysplasia | Aplastic Anemia | Lymphoma Lymphoblastic | Glycogen Storage Disease Type 0, Muscle | Panuveitis | Hyperekplexia | Spinocerebellar Ataxia Type 40 | Acute Lung Injury | Diabetic Encephalopathy | Retinoschisis | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Aarskog-Scott Syndrome | DiGeorge Syndrome | Raynaud Phenomenon | Motor Neuron Diseases | Pseudohypoparathyroidism Type 1C | Hepatorenal Syndrome | Angelman Syndrome | Graves Disease | Xeroderma Pigmentosum Variant Type | Adrenal Insufficiency | Cysticercosis | Ectodermal Dysplasia | Apparent Mineralocorticoid Excess Syndrome | Renal Failure | Spinocerebellar Ataxia Type 23 | 3-M Syndrome | Chondrodysplasia Punctata | Cramp Fasciculation Syndrome | Papilloma | Short-chain Acyl-CoA Dehydrogenase Deficiency | Hyperkalemic Periodic Paralysis | Disseminated Intravascular Coagulation | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Nail Disorder, Nonsyndromic Congenital | Coronary Artery Disease | Noonan Syndrome | Acrodermatitis Enteropathica | Progressive Familial Intrahepatic Cholestasis Type 1 | Gestational Trophoblastic Disease | Hypopituitarism | Pontocerebellar Hypoplasia Type 7 | Central Pain Syndrome | Deafness, Dystonia, And Cerebral Hypomyelination | Rift Valley Fever | Cardiomyopathy, Restrictive | Plasma Cell Leukemia | Loeys-Dietz Syndrome | Hyperbilirubinemia, Neonatal | Anosmia, Congenital | HELLP Syndrome | Pleurisy | Sweet Syndrome | Diabetic Neuropathy | Autism | Progressive Encephalopathy-optic Atrophy Syndrome | Adenoma, Pituitary | Pierson Syndrome | Aneurysm, Abdominal Aortic | Multiple System Atrophy | Thyroid Dysgenesis | Rhabdomyosarcoma, Alveolar | Dysthymia | Hemophagocytic Lymphohistiocytosis | Microphthalmia | Hyperparathyroidism, Primary | Lymphangiomatosis | Goiter, Nodular | C3 Glomerulonephritis | Obesity, Morbid | Non-bullous Congenital Ichthyosiform Erythroderma | Raine Syndrome | Roberts Syndrome | Glycogen Storage Disease Type 1a | Stuve-Wiedemann Syndrome | Oculodentodigital Dysplasia | Facioscapulohumeral Muscular Dystrophy Type 2 | Spinocerebellar Ataxia Type 7 | Cerebrotendinous Xanthomatosis | Cancer, Colon | Myopia | Conjunctivitis | Osteonecrosis | Smoldering Myeloma | Oligoasthenoteratozoospermia | Distal Myopathy 2 | Pfeiffer Syndrome | Acromesomelic Dysplasia | Spina Bifida | Carey-Fineman-Ziter Syndrome | Focal Segmental Glomerulosclerosis | Duchenne Muscular Dystrophy | Scleroderma, Diffuse | Anuria | Mast Cell Leukemia | Retinal Dystrophy, Early-onset Severe | Polycystic Ovary Syndrome | Non-Hodgkin Lymphoma | CHOPS Syndrome | T-cell Lymphoma, Subcutaneous Panniculitis-like | Cryptorchidism | Seminoma | Dysequilibrium Syndrome | Carcinoid Tumor | Dyslipidemia | Familial Dysautonomia | Spitz Nevus | Disseminated Superficial Actinic Porokeratosis | Nance-Horan Syndrome | Anovulation | Richter's Syndrome | Keratoconus | Mixed Connective Tissue Disease | Narcolepsy | Astrocytoma | Chorioretinitis | Primary Familial Brain Calcification | Crouzon Syndrome With Acanthosis Nigricans | Alpha-mannosidosis | Eclampsia | Juvenile Xanthogranuloma | Hypertension, Renal | Cholestasis, Intrahepatic | Vaginitis | Hemangioendothelioma | Insulinoma | Progressive External Ophthalmoplegia | Cornelia De Lange Syndrome | Bare Lymphocyte Syndrome | Hyperglycemia | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Cutaneous Lupus Erythematosus | Parkinsonism | Vitamin A Deficiency | Postaxial Polydactyly | Nanophthalmos | Diabetes Insipidus, Neurogenic | Congenital Adrenal Hyperplasia 1 | Cataplexy | Osteochondrosis | Diabetes | Parkinson Disease 6, Autosomal Recessive Early-onset | Mabry Syndrome | Adams-Oliver Syndrome | Metaphyseal Chondrodysplasia, Schmid Type | Mannosidase Deficiency Diseases | Hypotonia-cystinuria Syndrome | Babesiosis | Obsessive-compulsive Disorder | Kernicterus | Infantile Nephropathic Cystinosis | Hepatitis A | Adenosine Deaminase Deficiency | Arthritis, Gouty | Bulimia Nervosa | Oligoastrocytoma | Diabetes Gestational | Acute Generalized Exanthematous Pustulosis | Pancreatitis, Chronic | L-2-Hydroxyglutaric Aciduria | Crigler-Najjar Syndrome | Hepatic Steatosis | Angiomyolipoma | Diffuse Palmoplantar Keratoderma | Avellino Corneal Dystrophy | Eiken Syndrome | Seizures | Polycystic Kidney, Autosomal Dominant | Thyroid Hormone Resistance | Meningococcal Meningitis | Eosinophilia | Ghosal Syndrome | Cholera | Inflammatory Joint Disease | Extramammary Paget's Disease | Pemphigus | Takayasu's Arteritis | Fuchs Dystrophy | Leiomyoma | Optic Neuropathy, Anterior Ischemic | Spondyloperipheral Dysplasia | Creatine Deficiency Syndrome Due To AGAT Deficiency | Systemic Lupus Erythematosus | CHARGE Syndrome | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Hypopigmentation | Porphyria, Acute Intermittent | Hereditary Neuropathy With Liability To Pressure Palsies | Binge Eating Disorder | Eccrine Porocarcinoma | Pontocerebellar Hypoplasia Type 2 | Nephronophthisis | Vascular Cognitive Impairment | Polymicrogyria | Steel Syndrome | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Urea Cycle Disorder | Compartment Syndrome | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Hypolipoproteinemia | Asperger Syndrome | Learning Disability | Encephalopathy | Granular Corneal Dystrophy Type 1 | Marshall-Smith Syndrome | Cervical Dystonia | Autonomic Nervous System Disorders | Ganglioglioma | Microtia | Lentigo | Liddle Syndrome | Pterygium | Sialidosis | Sjogren Syndrome | Optic Nerve Hypoplasia, Bilateral | Pulmonary Vein Stenosis | Primary Aldosteronism | Aldosterone Synthase Deficiency | Lymphopenia | Non-Langerhans Cell Histiocytosis | Pulmonary Veno-occlusive Disease | Low Tension Glaucoma | Hemangioma | Essential Fructosuria | Parkinson's Disease | Farber Disease | Trismus-pseudocamptodactyly Syndrome | Atelosteogenesis Type 2 | Globozoospermia | Spinal Muscular Atrophy Type 3 | AIDS | Chronic Mucocutaneous Candidiasis | Microcephaly | Vitreoretinal Degeneration, Snowflake Type | Hyperthermia, Malignant | Cole-Carpenter Syndrome | Postpartum Depression | Greig Cephalopolysyndactyly Syndrome | Bullous Pemphigoid | Neurogenic Bladder | Lassa Fever | Premature Ejaculation | Myositis, Focal | Netherton Syndrome | Dupuytren Disease | Generalized Epilepsy With Febrile Seizures Plus | Carbonic Anhydrase VA Deficiency | Rickets | Cheilitis | Moyamoya Disease | Glaucoma, Congenital | Barrett Esophagus | Sarcoma, Alveolar Soft Part | Arthrogryposis | Stroke | Glioblastoma Multiforme | Corneal Ulcer | Wolcott-Rallison Syndrome | Gastroschisis | Retinal Vasculitis | Peeling Skin Syndrome Type B | Acute Lymphocytic Leukemia | Antenatal Bartter Syndrome Type 1 | Peripheral T-cell Lymphoma | Fragile X Syndrome | Meleda Disease | Spinocerebellar Ataxia | Neuroendocrine Cancer | Acute Myeloid Leukemia | Vulvovaginitis | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Treacher Collins Syndrome | Thrombophlebitis | Chylothorax, Congenital | Alagille Syndrome | Enhanced S-cone Syndrome | Otopalatodigital Syndrome Type 2 | Blepharoconjunctivitis | Charcot-Marie-Tooth Disease, Type 6 | Autosomal Recessive Spastic Paraplegia Type 75 | GAPO Syndrome | Hyperbilirubinemia | Pituitary Dwarfism | Walker-Warburg Syndrome | Malaria, Cerebral | Lafora Disease | Pneumoconiosis | Osteomyelitis | Hyperacusis | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Renal Tubular Dysgenesis | MIRAGE Syndrome | Chondrodysplasia Punctata 1, X-linked Recessive | Rolandic Epilepsy | 5-oxoprolinase Deficiency | Spondylocostal Dysostosis | Leprosy | Colitis | Pseudohermaphroditism | Coronary Heart Disease | Stargardt Disease | Pulmonary Stenosis | Hypersensitivity Pneumonitis | Loeys-Dietz Syndrome Type 4 | Peripheral Neuropathy | Sickle Cell Anemia | Familial Pheochromocytoma-paraganglioma | Lichen Sclerosus | Congenital Bile Acid Synthesis Defect | Hyperandrogenemia | Liver Failure | Congenital Hereditary Endothelial Dystrophy Type II | Neurodegeneration With Brain Iron Accumulation | Cryopyrin-associated Periodic Syndromes | Trichorhinophalangeal Syndrome | Phosphoglycerate Dehydrogenase Deficiency | Hyperlipidemia | Congenital Disorders Of Glycosylation Type II | Meningococcal Infections | Familial Glucocorticoid Deficiency | Mitochondrial DNA Depletion Syndrome 13 | Keratitis | Blau Syndrome | Pleural Tuberculosis