Disease

Holoprosencephaly

About the Disease
Holoprosencephaly, also known as holoprosencephaly sequence, is related to holoprosencephaly 9 and holoprosencephaly 7. An important gene associated with Holoprosencephaly is FGFR1 (Fibroblast Growth Factor Receptor 1), and among its related pathways/superpathways are Signal Transduction and Signaling by Hedgehog. Affiliated tissues include Primitive Streak, brain and eye, and related phenotypes are abnormal facial shape and holoprosencephaly

Common Targets
GLI2 | FAT1 | TGIF1 | SUFU | FGFR1 | SMC1A | PTCH1 | RAD21 | FGF8 | GAS1 | DISP1 | STIL | KMT2D | DLL1 | SHH | ZIC2 | SMC3 | PLCH1 | BOC | SIX3 | STAG2

疾病靶点研报
Holoprosencephaly

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

Other Diseases

Citrullinemia | T-cell Chronic Lymphocytic Leukemia | Wolfram Syndrome | Sturge-Weber Syndrome | Trigonocephaly | Hepatoblastoma | Twin-to-twin Transfusion Syndrome | Focal Dermal Hypoplasia | Greig Cephalopolysyndactyly Syndrome | Nephrotic Syndrome | Renal Failure | Inflammatory Linear Verrucous Epidermal Nevus | Tinea | Gastroschisis | Cystitis, Interstitial | Hermansky-Pudlak Syndrome | Pneumonia, Viral | Alpers Syndrome | Cardiomyopathy, Hypertrophic | Klinefelter Syndrome | Migraine | Craniolenticulosutural Dysplasia | Myotonic Disorders | Pneumococcal Meningitis | Eclampsia | Double Outlet Right Ventricle | Chondromyxoid Fibroma | Rhinitis | Blepharitis | Cold-induced Sweating Syndrome | Ophthalmoplegia | Spina Bifida | N-acetylglutamate Synthase Deficiency | Stuttering | Porphyria, Acute Intermittent | Charcot-Marie-Tooth Disease Type 2E | Esotropia | Dysthymia | Pericarditis | Osteogenesis Imperfecta Type III | Granular Corneal Dystrophy Type 1 | Cancer, Colon | Glycogen Storage Disease Type 0 | Atrial Septal Defect | Frontotemporal Dementia | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Insulin Resistance | Myoclonus-dystonia Syndrome | Lateral Meningocele Syndrome | Congenital Tufting Enteropathy | Melanoma, Uveal | Epidermolytic Palmoplantar Keratoderma | Barakat Syndrome | Keratitis | Avellino Corneal Dystrophy | Rothmund-Thomson Syndrome | Chordoma | Lipid Metabolism Disorders | Hereditary Inclusion Body Myopathy | Mabry Syndrome | Periodic Limb Movement Disorder | Renal Hypomagnesemia 3 | Premature Ejaculation | Melanocytic Nevus | Charcot-Marie-Tooth Disease Type 4D | Hyperekplexia | Silicosis | Meningioma, Benign | Rheumatic Heart Disease | Multiple Hamartoma Syndrome | Mannosidase Deficiency Diseases | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Combined Malonic And Methylmalonic Acidemia | Blepharo-cheilo-odontic Syndrome | McLeod Syndrome | Megaloblastic Anemia | Endophthalmitis | Fibrillation, Atrial | AIDS | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Recurrent Respiratory Papillomatosis | Danon Disease | Huntington's Disease-like 2 | Idiopathic Pulmonary Fibrosis | Pure Red Cell Aplasia | Spinocerebellar Ataxia Type 40 | Transcobalamin Deficiency | Anorexia Nervosa | Charcot-Marie-Tooth Disease, Type 2 | Dysequilibrium Syndrome | Jacobsen Syndrome | Eiken Syndrome | Chromosome 16p11.2 Deletion Syndrome | Asplenia | Vascular Cognitive Impairment | Hemolytic Uremic Syndrome, Atypical | Contact Dermatitis | Myocardial Infarction | Sporadic Inclusion Body Myositis | Lung Diseases | Neurofibrosarcoma | Fundus Albipunctatus | Spermatocele | GATA2 Deficiency | Prostatitis | Ependymoma | Nestor-Guillermo Progeria Syndrome | Epithelioid Hemangioma | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Williams Syndrome | Glycogen Storage Disease Type 1a | Hypokalemia | Thrombocytopenia | Schistosomiasis | Heterotopic Ossification | Hypocalcemia | Neonatal Progeroid Syndrome | Periventricular Leukomalacia | Heterotaxy | Specific Granule Deficiency | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Acute Chest Syndrome | Craniosynostosis | Orthostatic Intolerance | Erythromelalgia | Panic Disorder | Schwannomatosis | Johanson-Blizzard Syndrome | Obesity | Adrenal Insufficiency | Retinal Vasculitis | Primary Sclerosing Cholangitis | Thromboembolism | Klippel-Feil Syndrome | Prolidase Deficiency | Chondrodysplasia Punctata 1, X-linked Recessive | Avian Influenza | Craniofrontonasal Syndrome | Leukoencephalopathy, Progressive Multifocal | NDH Syndrome | X-linked Charcot-Marie-Tooth Disease | Anti-NMDA Receptor Encephalitis | Lipoma | Uremia | Melanoma, Malignant | Osteogenesis Imperfecta Type V | Dyslipidemia | Ectopia Lentis, Isolated, Autosomal Recessive | Spinocerebellar Ataxia Type 31 | Chronic Beryllium Disease | Pouchitis | Abetalipoproteinemia | Fuchs Heterochromic Iridocyclitis | Pityriasis Rubra Pilaris | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Hemochromatosis Type 1 | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Hypohidrotic Ectodermal Dysplasia | Pancreatitis, Chronic | Primary Erythromelalgia | Nance-Horan Syndrome | Achondrogenesis | Pulmonary Capillary Hemangiomatosis | Phosphoglycerate Dehydrogenase Deficiency | DNA Ligase IV Deficiency | Papilledema | Viral Meningitis | Adenoid Cystic Carcinoma | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Spinocerebellar Ataxia Type 23 | Schizoaffective Disorder | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Atherosclerosis | Myofibrillar Myopathy | Gastritis, Atrophic | Gestational Trophoblastic Disease | Facioscapulohumeral Muscular Dystrophy Type 2 | Malaria | Skin Papilloma | Congenital Poikiloderma | Aromatic L-amino Acid Decarboxylase Deficiency | Tetraplegia | Exotropia | Retinal Degeneration | Aarskog-Scott Syndrome | Thyroid Dysgenesis | Adams-Oliver Syndrome | Tenosynovial Giant Cell Tumor | 3-methylglutaconic Aciduria | Esophageal Adenocarcinoma | Hydrocephalus, Normal Pressure | Lesch-Nyhan Syndrome | Muckle-Wells Syndrome | Best Macular Dystrophy | Cutaneous Lupus Erythematosus | Chediak-Higashi Syndrome | Snyder-Robinson Syndrome | Benign Familial Infantile Seizures | Multiple System Atrophy | Mixed Connective Tissue Disease | Hemorrhagic Disorders | Miyoshi Myopathy | Cryptococcal Meningitis | Microcephaly, Seizures, And Developmental Delay | Reflex Epilepsy | Microvillus Inclusion Disease | Blue Nevus | Liver Failure, Acute Infantile | 5-oxoprolinase Deficiency | Teratozoospermia | Hypertensive Nephropathy | Hyperphenylalaninemia | Frank-ter Haar Syndrome | Androgenic Alopecia | Autoimmune Polyendocrinopathy Syndrome Type I | Paronychia | Thrombocythemia, Essential | Congenital Ichthyosiform Erythroderma | Aicardi-Goutieres Syndrome | Cheilitis | Stuve-Wiedemann Syndrome | Coffin-Siris Syndrome | Analgesia | Lentigo | Autonomic Neuropathy | Retinal Detachment | Hypohidrotic Ectodermal Dysplasia, X-linked | Carcinoma, Merkel Cell | Extramammary Paget's Disease | Acute Generalized Exanthematous Pustulosis | Oligoasthenoteratozoospermia | C3 Glomerulonephritis | Spinocerebellar Ataxia Type 14 | Spinocerebellar Ataxia Type 6 | Dysfibrinogenemia | Cancer, Skin | Acute Myeloid Leukemia | Antithrombin III Deficiency | Fibromyalgia | Pulmonary Sclerosing Hemangioma | Dentinogenesis Imperfecta | Neurofibromatosis | McKusick Type Metaphyseal Chondrodysplasia | HUPRA Syndrome | Sleep Disorder | Primary Familial Brain Calcification | Cholera | Cardiospondylocarpofacial Syndrome | Cystinuria | Lattice Corneal Dystrophy Type 1 | Otosclerosis | Hypertelorism | Methylmalonic Acidemia | Ichthyosis Bullosa Of Siemens | Familial Hyperaldosteronism | Werner's Syndrome | Lymphoma, Follicular | Apparent Mineralocorticoid Excess Syndrome | Cholestasis | Inflammatory Bowel Disease | Lymphopenia | Rhabdomyosarcoma, Embryonal | Cholecystitis | Budd-Chiari Syndrome | Waardenburg Syndrome Type 1 | Central Pain Syndrome | PHARC Syndrome | Crohn's Disease | Leishmaniasis, Cutaneous | Xeroderma Pigmentosum | Mucolipidosis Type III | Gastroenteritis | Adenocarcinoma | Sarcosinemia | Hypospadias | Hyperparathyroidism | Dermatitis Herpetiformis | Mitochondrial Cytopathy | Glycogen Storage Disease Type 0, Muscle | Shwachman-Bodian-Diamond Syndrome | Apraxia | Hyperlipidemia | Rift Valley Fever | Osteosarcoma | Mitochondrial Disease | Schuurs-Hoeijmakers Syndrome | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Diabetic Nephropathy | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Preaxial Polydactyly | Generalized Epilepsy With Febrile Seizures Plus | Burn-McKeown Syndrome | FG Syndrome | Long QT Syndrome Type 2 | Pseudohermaphroditism | Hepatitis, Autoimmune | Rosacea | Progressive Familial Intrahepatic Cholestasis | Hypolipoproteinemia | Pitt-Hopkins Syndrome | Ulcerative Colitis | Schizophrenia, Paranoid | Iron Deficiency Anemia | Progressive Osseous Heteroplasia | Papulopustular Rosacea | Polycystic Kidney, Autosomal Recessive | Primary Hyperoxaluria Type 1 | Hypertension, Pulmonary | Trachoma | GLUT1 Deficiency Syndrome | Perry Syndrome | Bardet-Biedl Syndrome | Hypercalcemia | Heart Septal Defects | Parkinson Disease 6, Autosomal Recessive Early-onset | Pendred Syndrome | Rhizomelic Chondrodysplasia Punctata | Phenylketonuria II | Geleophysic Dysplasia | Rickets | Leber Hereditary Optic Neuropathy | Panniculitis | Uremic Pruritus | Atopy | Infantile Neuroaxonal Dystrophy | Acne Vulgaris | Non-Hodgkin Lymphoma | Aspartylglycosaminuria | Paraganglioma, Carotid Body | Allan-Herndon-Dudley Syndrome | Esophageal Carcinoma | Carney-Stratakis Syndrome | Keratoconus | Glycogen Storage Disease Type 5 | Endometritis | Schindler Disease | Melnick-Needles Syndrome | Dyggve-Melchior-Clausen Disease | Galactosialidosis | Cholestasis, Intrahepatic | Ataxia-ocular Apraxia 2 | Myoclonic Atonic Epilepsy | 3-methylcrotonyl-CoA Carboxylase Deficiency | Disseminated Superficial Actinic Porokeratosis | Exfoliative Dermatitis | Granuloma Annulare | Fuchs Dystrophy | Bipolar Disorder | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Charcot-Marie-Tooth Disease Type 4B1 | Giant Cell Arteritis | Meningioma | Scabies | Nemaline Myopathy | Alopecia Totalis | Polycystic Kidney, Autosomal Dominant | Menkes Disease | Primary Carnitine Deficiency | Esophageal Motility Disorders | Pycnodysostosis | Carcinoma, Squamous Cell | Sezary Syndrome | Coronary Restenosis | Charcot-Marie-Tooth Disease, Type 2C | Silver-Russell Syndrome | Sickle Cell Anemia | Multicentric Carpotarsal Osteolysis Syndrome | Lassa Fever | Encephalopathy, Hepatic | Mumps | Gray Platelet Syndrome | Trichothiodystrophy | Charcot-Marie-Tooth Disease Axonal Type 2N | Canavan Disease | Familial Advanced Sleep Phase Syndrome | Opisthorchiasis | Trichuriasis | Warsaw Breakage Syndrome | Veno-occlusive Disease | Waardenburg Syndrome Type 4 | Dyskeratosis Congenita | Epidermolytic Ichthyosis, Annular | McCune-Albright Syndrome | Spinal Muscular Atrophy Type 2 | Agnathia-Otocephaly Complex | Glycogen Storage Disease Type 1 | Osteitis | Hepatorenal Syndrome | Colorectal Adenoma | Oculocutaneous Albinism Type 4 | Inborn Errors Of Metabolism | Carbamoyl Phosphate Synthetase I Deficiency | Beckwith-Wiedemann Syndrome | Netherton Syndrome | Carbohydrate Metabolism Disorders | Bronchiolitis | Cholangitis | Cryoglobulinemia | Ectrodactyly | Encephalocele