Disease

Alazami Syndrome

About the Disease
Alazami Syndrome, also known as microcephalic primordial dwarfism, alazami type, is related to alacrima, achalasia, and mental retardation syndrome and persistent hyperplastic primary vitreous, autosomal recessive. An important gene associated with Alazami Syndrome is LARP7 (La Ribonucleoprotein 7, Transcriptional Regulator). Affiliated tissues include eye, skin and bone, and related phenotypes are widely spaced teeth and intellectual disability, severe

Common Targets
LARP7

疾病靶点研报
Alazami Syndrome

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

Other Diseases

Carpenter Syndrome | Encephalopathy, Ethylmalonic | Pneumonia, Mycoplasma | Chondrosarcoma | Axenfeld-Rieger Syndrome | Congenital Poikiloderma | Riboflavin Transporter Deficiency Neuronopathy | Epicondylitis | Anencephaly | Glioma | Waardenburg Syndrome Type 2A | Transcobalamin Deficiency | Neonatal Progeroid Syndrome | Early Infantile Epileptic Encephalopathy 28 | Intracranial Hypertension | Mitochondrial Disease | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Melanoma | Lattice Corneal Dystrophy | Cancer, Prostate | Spinal Muscular Atrophy Type 3 | Lyme Disease | Choriocarcinoma | Cerebellofaciodental Syndrome | Herpes Genitalis | Scapuloperoneal Myopathy, X-linked Dominant | Obsessive-compulsive Disorder | Galloway-Mowat Syndrome | Hepatitis, Alcoholic | Ganglioneuroma | Early Infantile Epileptic Encephalopathy 1 | Coronary Restenosis | Iron Overload | Aromatic L-amino Acid Decarboxylase Deficiency | HIBCH Deficiency | Paracoccidioidomycosis | Hennekam Lymphangiectasia-lymphedema Syndrome | Mast Cell Leukemia | Carcinoma, Transitional Cell | Presbyopia | Nail Disorder, Nonsyndromic Congenital | Erythromelalgia | Acrodysostosis | Myocarditis | Pituitary Disorders | Thalassemia, Beta | Pontocerebellar Hypoplasia Type 2 | Dystonia Musculorum Deformans | Waardenburg Syndrome | Aarskog-Scott Syndrome | Atopy | Nicolaides-Baraitser Syndrome | Gray Platelet Syndrome | T-cell Leukemia | Anal Fissure | Bipolar Disorder | Macular Corneal Dystrophy | Spinocerebellar Ataxia Type 10 | Mitochondrial Cytopathy | Tricho-hepato-enteric Syndrome | Azoospermia | Lactose Intolerance | Vitamin K Deficiency | Seborrheic Dermatitis | Dysthymia | Stiff-man Syndrome | Hernia, Inguinal | Keratosis, Seborrheic | Membranous Nephropathy | Hypobetalipoproteinemias | Disseminated Superficial Actinic Porokeratosis | Basan Syndrome | Cardiomyopathy, Dilated, 1L | Olmsted Syndrome | Gastric Atrophy | Anti-glomerular Basement Membrane Disease | Tetraplegia | Adenoid Cystic Carcinoma | Nephropathy | Gerstmann-Straussler-Scheinker Syndrome | Hyperhomocysteinemia | Porphyria Cutanea Tarda | Jaundice, Obstructive | Familial Dysautonomia | Currarino Syndrome | Fanconi Syndrome | Asthma, Nocturnal | Long QT Syndrome Type 2 | Prolactinoma | Multicentric Carpotarsal Osteolysis Syndrome | Lipid Storage Myopathy | Optic Neuritis | Craniofrontonasal Syndrome | Antenatal Bartter Syndrome Type 1 | Cushing Syndrome | Congestive Heart Failure | Osteopetrosis | Epidermolysis Bullosa Simplex, Generalized | Pleomorphic Xanthoastrocytoma | Episodic Ataxia Type 1 | Urticaria | Osmotic Demyelination Syndrome | Cat Eye Syndrome | Ameloblastoma | Cancer, Skin | Macrophagic Myofasciitis | Spinocerebellar Ataxia Type 16 | Asthma | Congenital Heart Block | Early Infantile Epileptic Encephalopathy 4 | Episodic Ataxia Type 2 | Cholestasis, Intrahepatic | Erythropoietic Protoporphyria | Peyronie's Disease | Large Granular Lymphocytic Leukemia | Preaxial Polydactyly | Thyroid Hormone Resistance | Epidermal Nevus Syndrome | Ganglioglioma | Sarcoma, Alveolar Soft Part | Rhabdoid Tumor | Von Hippel-Lindau Disease | Hepatitis A | Neurofibroma, Plexiform | Juvenile Xanthogranuloma | Arthrogryposis | Hypertelorism | Congenital Afibrinogenemia | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Pericarditis | Corneal Dystrophies, Hereditary | Wolfram Syndrome 2 | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Basal Ganglia Cerebrovascular Disease | Myhre Syndrome | Cheilitis | Hyperekplexia | Adenomatoid Tumor | Anuria | Oligodendroglioma | Tinea Versicolor | Malaria, Cerebral | Antisynthetase Syndrome | Vascular Calcification | Glaucoma, Congenital | Cohen Syndrome | Abetalipoproteinemia | Hepatitis C, Chronic | Absence Epilepsy | Vitamin D Deficiency | Alpha-thalassemia Myelodysplasia Syndrome | Sertoli Cell-only Syndrome | Dysmorphophobia | Nemaline Myopathy | Blue Nevus | Gastritis, Atrophic | Diabetes Type 2 | Giant Axonal Neuropathy | Kleine-Levin Syndrome | Glutaric Aciduria Type 3 | Aldosteronism | Optic Neuropathy | Nephrocalcinosis | Adenocarcinoma | Restless Legs Syndrome | Progressive Myoclonic Epilepsy | Non-small Cell Lung Cancer | Sarcosinemia | Epilepsy Of Infancy With Migrating Focal Seizures | Common Cold | Proteus Syndrome | Chondrodysplasia Punctata | Hemangioma | Common Variable Immunodeficiency | Panniculitis | Charcot-Marie-Tooth Disease Type 2D | Chitayat Syndrome | Mandibuloacral Dysplasia With Type A Lipodystrophy | Liver Diseases | Schizophrenia, Paranoid | Glycogen Storage Disease Type 0, Muscle | Pityriasis Rubra Pilaris | Congenital Stromal Corneal Dystrophy | Burn-McKeown Syndrome | Spondylocarpotarsal Synostosis Syndrome | Smith-Magenis Syndrome | Turner's Syndrome | Hypertension, Renovascular | GLUT1 Deficiency Syndrome | Lymphoma, B-cell | Ornithine Transcarbamylase Deficiency | Glycogen Storage Disease Type 1 | Aicardi-Goutieres Syndrome | Branchiootorenal Syndrome | Hypotrichosis | Paternal Uniparental Disomy Of Chromosome 14 | Otitis Media | Cluster Headache | Pierre Robin Syndrome | 3-methylglutaconic Aciduria Type IV | Congenital Adrenal Hyperplasia | Paraplegia | Bone Marrow Necrosis | Peroxisomal Disorder | Prediabetes | Macrodactyly | C3 Glomerulopathy | Periodontitis | Ollier Disease | Micropenis | Relapsing Polychondritis | Astrocytoma, Anaplastic | Exotropia | Pleurisy | Alkaptonuria | Neurodegeneration With Brain Iron Accumulation | Pompe Disease | Lafora Disease | Nager Acrofacial Dysostosis | Supravalvular Aortic Stenosis | Graft-versus-host Disease | Neurofibromatosis Type 2 | Polymicrogyria | Seminoma | Spermatocele | Hypopigmentation | Congenital Hemolytic Anemia | Sjogren Syndrome | GNE Myopathy | Osteomyelitis | Hypoproteinemia, Hypercatabolic | Intracerebral Hemorrhage | Chondroma | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Fragile X Syndrome | Leukocyte Adhesion Deficiency Type 1 | Hyperparathyroidism, Secondary | ICF Syndrome | Hypercalciuria | Camurati-Engelmann Disease | Diamond-Blackfan Anemia | Senior-Loken Syndrome | Cyclic Vomiting Syndrome | Chondrodysplasia Punctata 1, X-linked Recessive | Moyamoya Disease | ACTH-independent Macronodular Adrenal Hyperplasia | Cabezas Syndrome | Primary Progressive Aphasia | Sialidosis Type I | Neutropenia | Measles | Arthritis, Reactive | Methylmalonic Acidemia | Lymphoma Lymphoblastic | Thanatophoric Dysplasia Type 1 | Mitochondrial Myopathy | Takayasu's Arteritis | Ehlers-Danlos Syndrome | Proteasome-associated Autoinflammatory Syndrome 2 | Pre-eclampsia | Congenital Dyserythropoietic Anemia Type 1 | Sengers Syndrome | Myelitis | Krabbe Disease | Heart Block | Narcolepsy | Glutathione Synthetase Deficiency | Phosphoglycerate Dehydrogenase Deficiency | Paget's Disease Of The Breast | Optic Atrophy 2 | Charcot-Marie-Tooth Disease, Type 2C | Zygomycosis | Myoclonic Atonic Epilepsy | Glycogen Storage Disease Type 1b | Malignant Peripheral Nerve Sheath Tumor | Loeys-Dietz Syndrome Type 4 | Raine Syndrome | Cataract | Hamartoma | Hereditary Spherocytosis | Glycogen Storage Disease Type 9 | Achromatopsia | Familial Episodic Pain Syndrome | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Mycosis Fungoides | Rothmund-Thomson Syndrome | Parkinson's Disease | Neurofibromatosis-Noonan Syndrome | Milk Allergy | Rubeosis Iridis | Paroxysmal Nocturnal Hemoglobinuria | Bartsocas-Papas Syndrome | Mabry Syndrome | Bacterial Meningitis | Charcot-Marie-Tooth Disease Axonal Type 2N | LMNA-related Congenital Muscular Dystrophy | Ocular Albinism Type 1 | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Autism Spectrum Disorders | Bronchitis, Chronic | Nutrition Disorders | Chanarin-Dorfman Syndrome | Schamberg Disease | Spondylolisthesis | Spinal Muscular Atrophy Type 2 | Esthesioneuroblastoma | Neutrophilia | Centronuclear Myopathy | Hypervalinemia | Osteosclerosis | Juvenile Polyposis | Hemosiderosis | Congenital Myasthenic Syndrome | MIRAGE Syndrome | Mucolipidosis Type II | Campomelic Dysplasia | Vestibular Disease | Multiple Epiphyseal Dysplasia | Cutaneous T-cell Lymphoma | Botulism | Enhanced S-cone Syndrome | Meningococcal Meningitis | Metabolic Diseases | Familial Partial Lipodystrophy | Synpolydactyly | Congenital Sodium Diarrhea | Dyskeratosis Congenita | Diabetic Macular Edema | Cervical Dystonia | Encephalopathy | Hemochromatosis | Chordoma | Arthropathy | Schistosomiasis Mansoni | NDH Syndrome | Kashin-Beck Disease | Chromosome 5q Deletion Syndrome | Subcortical Band Heterotopia | Niemann-Pick Disease | Odonto-onycho-dermal Dysplasia | Hypertension, Pulmonary | Fuchs Heterochromic Iridocyclitis | Spinocerebellar Ataxia Type 1 | Spinocerebellar Ataxia Type 38 | Carcinoid Tumor | Amebiasis | Schizoaffective Disorder | Presbycusis | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Schnyder Crystalline Corneal Dystrophy | Hyperkalemic Periodic Paralysis | Guillain-Barre Syndrome | GAPO Syndrome | McLeod Syndrome | Alcoholism | Motion Sickness | Donnai-Barrow Syndrome | Crigler-Najjar Syndrome | Melanocytic Nevus | Hypertensive Retinopathy | Paronychia | Neuroendocrine Cancer | MELAS Syndrome | Fontaine Progeroid Syndrome | Acromesomelic Dysplasia | Stickler Syndrome | Obesity | Coma | Carney-Stratakis Syndrome | L-2-Hydroxyglutaric Aciduria | Hepatopulmonary Syndrome | Peeling Skin Syndrome Type B | Iron Metabolism Disorders | Fundus Albipunctatus | Tuberculous Meningitis | Jawad Syndrome | Multiple System Atrophy | Lymphomatoid Granulomatosis | Encephalocele | Primary Hyperoxaluria Type 1 | Ocular Hypertension | Isovaleric Acidemia | Ataxia-ocular Apraxia 2 | Pemphigoid | Cardiomyopathy, Hypertrophic | Familial Hypertrophic Cardiomyopathy | Whipple's Disease | Scoliosis | DRESS Syndrome | Rhinitis | Pseudohermaphroditism | Pure Autonomic Failure | Myelitis, Transverse | Exocrine Pancreatic Insufficiency | Gout | Autoimmune Disease | Charcot-Marie-Tooth Disease Type 4B1 | Sarcoidosis, Pulmonary | Lymphoma | Opisthorchiasis