Pseudoachondroplasia
Pseudoachondroplasia
About the Disease
Pseudoachondroplasia, also known as pseudoachondroplastic dysplasia, is related to epiphyseal dysplasia, multiple, 1 and cartilage disease, and has symptoms including ulnar deviation of the wrist and waddling gait. An important gene associated with Pseudoachondroplasia is COMP (Cartilage Oligomeric Matrix Protein), and among its related pathways/superpathways are Integrin Pathway and Phospholipase-C Pathway. The drugs Resveratrol and Protective Agents have been mentioned in the context of this disorder. Affiliated tissues include bone and bone marrow, and related phenotypes are disproportionate short-limb short stature and waddling gait
Common Targets
COMP | DMD

Note: If you'd like to get a target analysis report for Pseudoachondroplasia, 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 Pseudoachondroplasia at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.tech.
Other Diseases
Low Phospholipid Associated Cholelithiasis | Light Chain Amyloidosis | Riboflavin Transporter Deficiency Neuronopathy | Glioblastoma | Basal Ganglia Disease, Biotin-responsive | Sialidosis | Heroin Dependence | Charcot-Marie-Tooth Disease, Type 6 | Multiple Sulfatase Deficiency | Neurofibromatosis | Hyperkeratosis | Kleine-Levin Syndrome | Hartsfield Syndrome | Crisponi Syndrome | Cerebrotendinous Xanthomatosis | Spinocerebellar Ataxia Type 1 | Crohn's Disease | Osteosclerosis | Chondrodysplasia Punctata 2, X-linked Dominant | Wolff-Parkinson-White Syndrome | Paronychia | Blau Syndrome | Left Ventricular Noncompaction | Autonomic Neuropathy | Glutaric Aciduria Type 2 | Primary Erythromelalgia | Oligoastrocytoma | Pancreatitis | Van Der Knaap Disease | Polymicrogyria | Methemoglobinemia | Christianson Syndrome | Infantile Nephropathic Cystinosis | Creatine Deficiency Syndrome Due To AGAT Deficiency | Tibial Muscular Dystrophy | Multicystic Renal Dysplasia | Gastrointestinal Disorders | Microtia | Low Tension Glaucoma | Epilepsy Of Infancy With Migrating Focal Seizures | Angioedema, Acquired | Chronic Enteropathy Associated With SLCO2A1 Gene | 3C Syndrome | Cardiomyopathy, Dilated, 1L | Creutzfeldt-Jakob Disease | Infantile Refsum Disease | Demyelinating Diseases | Mitochondrial DNA Depletion Syndrome 13 | Glycogen Storage Disease | Thyroid Hormone Resistance | Congenital Dyserythropoietic Anemia Type 1 | Ichthyosis Bullosa Of Siemens | Acute Anterior Uveitis | DNA Ligase IV Deficiency | Short-chain Acyl-CoA Dehydrogenase Deficiency | Juvenile Myelomonocytic Leukemia | Pyoderma Gangrenosum | Birk-Barel Syndrome | Leukodystrophies | Ectodermal Dysplasia | Epicondylitis | Pyruvate Decarboxylase Deficiency | Recurrent Respiratory Papillomatosis | Sialidosis Type I | Porphyria, Acute Intermittent | Renal Tubular Dysgenesis | Interstitial Lung Diseases | Oral Lichen Planus | Congenital Central Hypoventilation Syndrome | Angiosarcoma Of The Breast | Esophageal Adenocarcinoma | Bone Marrow Necrosis | Epidermodysplasia Verruciformis | Infantile Spasm | Takenouchi-Kosaki Syndrome | Anorexia Nervosa | Paracoccidioidomycosis | Nestor-Guillermo Progeria Syndrome | Spinocerebellar Ataxia Type 6 | Dysmorphophobia | Lymphopenia | Hepatitis C, Chronic | Conduct Disorder | Anemia | Trichotillomania | Lipid Storage Myopathy | Osteonecrosis Of The Jaw | Hyperostosis | Spinocerebellar Ataxia Type 21 | Chondroma | Brugada Syndrome 1 | Adenoma, Pituitary | Myelofibrosis | Familial Pheochromocytoma-paraganglioma | Hereditary Folate Malabsorption | Hypodontia | Ureteropelvic Junction Obstruction | Ventricular Septal Defect | Alpha-mannosidosis | Dupuytren Disease | Arteriosclerosis | Blastomycosis | Pulmonary Alveolar Microlithiasis | Skin Papilloma | Nephropathy | Thyroiditis | Gingivitis | Peutz-Jeghers Syndrome | Multiple Hamartoma Syndrome | Tendinopathy | Echinococcosis | Olmsted Syndrome | Congenital Absence Of Vas Deferens | 3-methylcrotonyl-CoA Carboxylase Deficiency | Otosclerosis | Progressive Myoclonic Epilepsy | Rotor Syndrome | Vitamin B12 Deficiency | Cutis Laxa | Anorectal Malformations | Rhabdoid Tumor | Tendinitis | Oligodendroglioma | Charcot-Marie-Tooth Disease Type 3 | Bone Giant Cell Tumor | Crigler-Najjar Syndrome | Eosinophilia | Neuromuscular Disorders | Cocaine-Related Disorders | Branchiootorenal Syndrome | Lichen Sclerosus | Renal Tubular Acidosis | Familial Exudative Vitreoretinopathy | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Uremia | Colitis, Collagenous | Metanephric Adenoma | Bietti Crystalline Dystrophy | Charcot-Marie-Tooth Disease Axonal Type 2N | Acrodermatitis Enteropathica | Focal Segmental Glomerulosclerosis | Acromicric Dysplasia | Cataract | Infertility | Thalassemia, Beta | Granuloma Annulare | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Retinal Detachment | Prurigo Nodularis | Arthritis, Psoriatic | Carotid Artery Disease | Retinal Coloboma | Acute Leukemia | B-cell Prolymphocytic Leukemia | Mood Disorder | Leukocyte Adhesion Deficiency Type 1 | Cardiac Arrest | Osteogenesis Imperfecta Type I | Spina Bifida | Subcortical Band Heterotopia | Vogt-Koyanagi-Harada Syndrome | Traboulsi Syndrome | Apert Syndrome | Specific Granule Deficiency | Temtamy Preaxial Brachydactyly Syndrome | Geleophysic Dysplasia | Hypopigmentation | Bruck Syndrome | Congenital Heart Defects | Carcinoma, Merkel Cell | Neutrophilia | Cherubism | Hyperoxaluria | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Meier-Gorlin Syndrome | Acrodysostosis | Myoclonus | Dysferlinopathy | Rhinitis | Orotic Aciduria | Aldosterone Deficiency | Amyotrophic Lateral Sclerosis | Primary Lateral Sclerosis | Cryoglobulinemia | Loeys-Dietz Syndrome | Autosomal Recessive Spastic Paraplegia Type 35 | Hyperinsulinemic Hypoglycemia | Vasculitis | Congenital Afibrinogenemia | Erdheim-Chester Disease | Nager Acrofacial Dysostosis | Gastritis, Atrophic | Hypotension, Orthostatic | Mohr-Tranebjaerg Syndrome | Pseudohypoparathyroidism Type 1A | Distal Myopathy 2 | Familial Cerebral Amyloid Angiopathy | Neutropenia | Basal Cell Nevus Syndrome | Carbonic Anhydrase VA Deficiency | Chorea | Epilepsy, Generalized | Blood Protein Disorders | Neurodermatitis | Occipital Neuralgia | Lattice Corneal Dystrophy Type 1 | Phenylketonuria II | Retinopathy, Diabetic | Pelizaeus-Merzbacher Disease | Rothmund-Thomson Syndrome | Anorchia | Lymphangioma | Bethlem Myopathy | Juvenile Xanthogranuloma | Muscular Dystrophy | Pyelonephritis | Glycogen Storage Disease Type 3 | Pierpont Syndrome | Focal Dermal Hypoplasia | Pre-eclampsia | Pyruvate Kinase Deficiency | Hyperekplexia | Autosomal Recessive Bestrophinopathy | Cerebrovascular Disorders | Japanese Encephalitis | Familial Thoracic Aortic Aneurysm | Neurofibromatosis Type 1 | DOCK8 Immunodeficiency Syndrome | Sporadic Hemiplegic Migraine | Cryptosporidiosis | Pseudohypoparathyroidism Type 2 | Whipple's Disease | Microcephalic Primordial Dwarfism | Polycystic Kidney, Autosomal Recessive | Glycogen Storage Disease Type 0 | Iron Deficiency Anemia | Oguchi Disease-2 | Acute Lung Injury | Milk Allergy | Oculopharyngeal Muscular Dystrophy | Tatton-Brown-Rahman Syndrome | Primary Pigmented Nodular Adrenocortical Disease | Homocystinuria | Melanocytic Nevus | Pendred Syndrome | Frank-ter Haar Syndrome | Anal Fissure | Nemaline Myopathy 10 | Methylmalonic Aciduria And Homocystinuria, CblC Type | Restless Legs Syndrome | Hemosiderosis | Brooke-Spiegler Syndrome | Spermatocele | Erectile Dysfunction | Schnitzler Syndrome | Hereditary Pyropoikilocytosis | Porokeratosis | Infantile Neuroaxonal Dystrophy | Ataxia-ocular Apraxia 2 | Acrocallosal Syndrome | Trachoma | Keratosis, Seborrheic | Personality Disorders | Amelanotic Melanoma | Central Pain Syndrome | Prostatitis | Hepatitis | Posterior Polar Cataract | Lymphomatoid Granulomatosis | Schizoaffective Disorder | Progressive Encephalopathy-optic Atrophy Syndrome | Hypersensitivity Pneumonitis | Adrenomyeloneuropathy | Costello Syndrome | Growth Hormone Excess | Retinal Dystrophy | Discoid Lupus Erythematosus | COACH Syndrome | Acne | Sleep Apnea | Multiple Myeloma | Pterygium | Jaundice, Obstructive | Cutaneous T-cell Lymphoma | Neurofibromatosis Type 2 | Chronic Neutrophilic Leukemia | Vulvovaginitis | Waardenburg Syndrome Type 2A | Pneumonia, Mycoplasma | Patent Foramen Ovale | Autosomal Recessive Spastic Paraplegia Type 54 | Xeroderma Pigmentosum Variant Type | Hepatorenal Syndrome | Osteoglophonic Dysplasia | Neuronal Ceroid Lipofuscinosis | Autosomal Recessive Congenital Ichthyosis | Familial Hypertrophic Cardiomyopathy | Intestinal Pseudo-obstruction | Coffin-Lowry Syndrome | Primary Sclerosing Cholangitis | Insulin Resistance | Schistosomiasis | Marinesco-Sjogren Syndrome | Protein S Deficiency | Retinitis Pigmentosa 3 | Multiple Sclerosis, Relapsing-remitting | Hyperphenylalaninemia | Giant Cell Arteritis | Chondrosarcoma | Trismus-pseudocamptodactyly Syndrome | Congenital Bile Acid Synthesis Defect | Ameloblastoma | Focal Facial Dermal Dysplasia | Gliosarcoma | Vitamin A Deficiency | Blomstrand Osteochondrodysplasia | Cyst | Anthrax | Waardenburg Syndrome | Temporal Lobe Epilepsy | Motor Neuron Diseases | Common Cold | Familial Dysautonomia | Carney Triad | Chronic Beryllium Disease | Galactosialidosis | Hydrolethalus Syndrome | Congenital Muscular Dystrophy | Dwarfism | Diabetic Macular Edema | Acute Generalized Exanthematous Pustulosis | Gout | Hepatic Adenomatosis | Sclerosteosis 2 | Corticobasal Syndrome | Hypocalcemia | Stickler Syndrome | Plasma Cell Leukemia | Progressive Familial Intrahepatic Cholestasis Type 2 | Phosphoglycerate Dehydrogenase Deficiency | Carpenter Syndrome | Cohen Syndrome | Chronic Kidney Disease | Stomatitis | Conn Syndrome | Hypertension, Pulmonary | Impulse Control Disorder | Paroxysmal Kinesigenic Dyskinesia | Distal Myopathy | Liddle Syndrome | Pancreatitis, Chronic | Hyperthermia, Malignant | Hepatic Veno-occlusive Disease | Mast Cell Leukemia | Blepharitis | Hypogonadism | Intestinal Tuberculosis | Anorectal Fistula | Polycystic Kidney, Autosomal Dominant | Sickle Cell Disease | Aplasia Cutis Congenita | Oculocutaneous Albinism | Hypertension, Essential | GM2-gangliosidosis AB Variant | Tumoral Calcinosis | Purpura | Pemphigoid | Dyslipidemia | Noonan Syndrome | Smith-Lemli-Opitz Syndrome | Spinal Muscular Atrophy Type 2 | Adenosine Deaminase Deficiency | Anovulation | X-linked Sideroblastic Anemia | Heart Failure | Craniofrontonasal Syndrome | Fundus Albipunctatus | Leiomyosarcoma | Keratitis-ichthyosis-deafness Syndrome | Hyperparathyroidism-jaw Tumor Syndrome | Prediabetes | Hyperacusis | Epidermolysis Bullosa | Cluster Headache | Seborrheic Dermatitis | Kabuki Syndrome | Charcot-Marie-Tooth Disease, Type 2 | Congenital Dyserythropoietic Anemia Type 4 | Mitochondrial Cytopathy | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Neurofibrosarcoma | Pleurisy | Premature Ejaculation | Sepiapterin Reductase Deficiency | Okihiro Syndrome | Cerebral Amyloid Angiopathy | Neuroectodermal Tumors, Primitive | Lipid Storage Diseases | Hereditary Neuropathy With Liability To Pressure Palsies | Hypokalemia