Congenital Central Hypoventilation Syndrome
Congenital Central Hypoventilation Syndrome
About the Disease
Congenital Central Hypoventilation Syndrome, also known as haddad syndrome, is related to central hypoventilation syndrome, congenital, 1 and hirschsprung disease 1. An important gene associated with Congenital Central Hypoventilation Syndrome is PHOX2B (Paired Like Homeobox 2B), and among its related pathways/superpathways are Signal Transduction and GDNF-Family Ligands and Receptor Interactions. The drugs Desogestrel and Contraceptives, Oral, Hormonal have been mentioned in the context of this disorder. Affiliated tissues include eye, colon and heart, and related phenotypes are failure to thrive and respiratory insufficiency
Common Targets
LBX1 | PHOX2B | MYO1H

Note: If you'd like to get a target analysis report for Congenital Central Hypoventilation 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 Congenital Central Hypoventilation Syndrome at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.tech.
Other Diseases
Tyrosinemia Type 1 | Pulmonary Capillary Hemangiomatosis | Renal Tubular Dysgenesis | Metachromatic Leukodystrophy | Primary Torsion Dystonia | Polycythemia Vera | Methemoglobinemia Type IV | PHARC Syndrome | Hypopituitarism | Esophageal Adenocarcinoma | Hyperlipidemia Type V | Ornithine Transcarbamylase Deficiency | Fanconi Anemia | Gastrointestinal Disorders | Mumps | Congenital Central Hypoventilation Syndrome | KBG Syndrome | Johanson-Blizzard Syndrome | Neurofibromatosis-Noonan Syndrome | Atopic Dermatitis | Aldosteronism | Smith-Lemli-Opitz Syndrome | Glycogen Storage Disease Type 5 | Hypertrophy | Hyperparathyroidism-jaw Tumor Syndrome | Combined Malonic And Methylmalonic Acidemia | Hyperbilirubinemia | Kabuki Syndrome 2 | Niemann-Pick Disease | Dementia | Thrombophilia | Cystitis | Lysosomal Acid Lipase Deficiency | Pseudoachondroplasia | Panic Disorder | Pituitary Stalk Interruption Syndrome | Chondroma | Syndactyly | Barrett Esophagus | Rubinstein-Taybi Syndrome | Blood Protein Disorders | Hypophosphatasia | Osteitis | Peutz-Jeghers Syndrome | Pure Red Cell Aplasia | Stroke, Hemorrhagic | Generalized Epilepsy With Febrile Seizures Plus | Blepharo-cheilo-odontic Syndrome | Familial Pheochromocytoma-paraganglioma | Oculodentodigital Dysplasia | Congenital Stromal Corneal Dystrophy | Spondyloperipheral Dysplasia | Angiosarcoma Of The Breast | Skin Papilloma | Patent Ductus Arteriosus | SAPHO Syndrome | Protein S Deficiency | Pierson Syndrome | Geleophysic Dysplasia | Cryptorchidism | HANAC Syndrome | Nephrocalcinosis | Diabetes Mellitus, Transient Neonatal | Amblyopia | Patent Foramen Ovale | Tatton-Brown-Rahman Syndrome | Gliosarcoma | Congenital Lipoid Adrenal Hyperplasia | Esotropia | Hypercalciuria | Glutaric Aciduria Type 2 | X-linked Myotubular Myopathy | Amyloidosis | Congenital Disorders Of Glycosylation | Inflammatory Myopathy | Ectopia Lentis, Isolated, Autosomal Recessive | Antisocial Personality Disorder | Metabolic Syndrome | Guttate Psoriasis | Pneumonia, Mycoplasma | Ocular Albinism Type 1 | Sepiapterin Reductase Deficiency | Congenital Poikiloderma | Thromboembolism | Spinocerebellar Ataxia Type 15 | Adult Polyglucosan Body Disease | Kashin-Beck Disease | Neuroblastoma | Epidermolysis Bullosa Simplex | Hepatoblastoma | Blepharitis | Cherubism | Methylmalonic Aciduria And Homocystinuria, CblC Type | Hepatitis | Carcinoma, Small Cell | Lymphomatoid Granulomatosis | Neuroectodermal Tumors, Primitive | Retinal Coloboma | H Syndrome | Hyperkeratosis | Microcephaly, Seizures, And Developmental Delay | Blomstrand Osteochondrodysplasia | Schwartz-Jampel-Aberfeld Syndrome | Keratitis-ichthyosis-deafness Syndrome | Juvenile Myelomonocytic Leukemia | Postpoliomyelitis Syndrome | Cancer, Breast | Conn Syndrome | Corneal Neovascularization | Spondylocostal Dysostosis | Glycogen Storage Disease Type 4 | Nevus | Chronic Inflammatory Demyelinating Polyneuropathy | Cervical Dystonia | Seasonal Mood Disorder | Tremor | Myeloid Leukemia | Aromatic L-amino Acid Decarboxylase Deficiency | Li-Fraumeni Syndrome | Hartnup Disease | Acrodysostosis | Zimmermann-Laband Syndrome | 3-methylglutaconic Aciduria Type IV | Cancer, Prostate | Histiocytosis | Diastrophic Dysplasia | Liver Failure, Acute Infantile | Mastitis | Alopecia | Chudley-McCullough Syndrome | Huntington's Disease | Presbyopia | Coronary Restenosis | Hypodontia | Early Infantile Epileptic Encephalopathy 1 | Arts Syndrome | Distal Spinal Muscular Atrophy | Retinitis | DiGeorge Syndrome | Charcot-Marie-Tooth Disease Type 4 | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Carbonic Anhydrase VA Deficiency | Pregnancy, Ectopic | Palmoplantar Keratoderma | Priapism | Spinocerebellar Ataxia Type 3 | Ischemia | Autoimmune Disease | Addison Disease | Major Depression | Pseudohermaphroditism | Uremia | Anovulation | Congenital Myasthenic Syndrome | Intestinal Hypomagnesemia 1 | Epilepsy, Generalized | Pituitary Disorders | Episodic Ataxia Type 1 | Stevens-Johnson Syndrome | Cockayne Syndrome | Heart Block | Hereditary Mixed Polyposis Syndrome | GLUT1 Deficiency Syndrome | Small Lymphocytic Lymphoma | Ameloblastoma | Pigment Dispersion Syndrome | Lipoma | Lymphoma, AIDS-related | Binge Eating Disorder | Crohn's Disease | Gastroschisis | Erythromelalgia | Glycogen Storage Disease Type 0, Muscle | Tricho-hepato-enteric Syndrome | Conduct Disorder | Yellow Fever | Psoriasis | Hyperparathyroidism, Secondary | Neuronal Ceroid Lipofuscinosis | Rhabdoid Tumor | CEDNIK Syndrome | Adenylosuccinate Lyase Deficiency | Hepatitis, Alcoholic | Anxiety Disorders | Infantile Nephropathic Cystinosis | Pycnodysostosis | Acrocallosal Syndrome | Chediak-Higashi Syndrome | Spinocerebellar Ataxia Type 6 | Prader-Willi Syndrome | Vaginitis | Adenoma, Pleomorphic | Hypoproteinemia, Hypercatabolic | Polymyalgia Rheumatica | Spondylocarpotarsal Synostosis Syndrome | Delayed Sleep Phase Syndrome | Chondrodysplasia Punctata 2, X-linked Dominant | Lymphoproliferative Disease, X-linked | Ulcerative Colitis | Hemimegalencephaly | Mosaic Variegated Aneuploidy Syndrome 2 | Sensorineural Hearing Loss | Anodontia | Parvovirus B19 Infection | Spinocerebellar Ataxia Type 20 | Hyperthyroidism | Infectious Diarrhea | Peters-plus Syndrome | Basal Cell Nevus Syndrome | Methemoglobinemia | Isovaleric Acidemia | Sarcoidosis, Pulmonary | Hypohidrotic Ectodermal Dysplasia, X-linked | Delirium | Amebiasis | Pontocerebellar Hypoplasia Type 7 | Cysticercosis | Wolfram Syndrome 2 | Krabbe Disease | Choroideremia | Guillain-Barre Syndrome | Hepatitis C, Chronic | Hypocalcemia | Pseudomyxoma Peritonei | Antenatal Bartter Syndrome Type 1 | 5-oxoprolinase Deficiency | Blue Rubber Bleb Nevus Syndrome | Basal Ganglia Disease, Biotin-responsive | Optic Atrophy 2 | Ventricular Septal Defect | Kallmann Syndrome | Loeys-Dietz Syndrome Type 4 | Schizoaffective Disorder | Spitz Nevus | Hepatic Adenomatosis | Mucolipidosis Type III | Uveitis, Anterior | Mood Disorder | DEND Syndrome | Depression | Moyamoya Disease | HELLP Syndrome | Bicuspid Aortic Valve | Transcobalamin Deficiency | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Traboulsi Syndrome | Hepatitis D | Familial Exudative Vitreoretinopathy | Pneumoconiosis | Pleural Tuberculosis | Pancreatitis, Chronic | LMNA-related Congenital Muscular Dystrophy | Isobutyryl-CoA Dehydrogenase Deficiency | Familial Hemiplegic Migraine | Hamartoma | Riboflavin Transporter Deficiency Neuronopathy | Pancytopenia | Erdheim-Chester Disease | Bietti Crystalline Dystrophy | Liddle Syndrome | Muckle-Wells Syndrome | Ependymoma | Subcortical Band Heterotopia | Proximal Symphalangism | Astrocytoma, Anaplastic | Paronychia | Cerebellofaciodental Syndrome | Pitt-Hopkins Syndrome | Lymphoma, Mantle Cell | HIBCH Deficiency | Takotsubo Cardiomyopathy | Erythema Multiforme | Guanidinoacetate Methyltransferase Deficiency | Low Phospholipid Associated Cholelithiasis | Spasticity | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Hyperprolactinemia | Menetrier Disease | Periventricular Nodular Heterotopia | Mitochondrial DNA Depletion Syndrome | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Inflammatory Myofibroblastic Tumor | Familial Glucocorticoid Deficiency | Gestational Trophoblastic Disease | Distal Myopathy 2 | IgA Nephropathy | LEOPARD Syndrome | Diabetes Insipidus | Usher Syndrome Type II | Congenital Bilateral Absence Of Vas Deferens | Learning Disability | Filariasis | Arteriovenous Malformations | Proctitis | Schaaf-Yang Syndrome | Atelosteogenesis Type 2 | Constipation | Pineoblastoma | Vascular Cognitive Impairment | Graves Disease | Corneal Dystrophy And Perceptive Deafness | Lipid Storage Diseases | Cancer, Brain | Hereditary Multiple Exostoses | Acne | Oligoasthenoteratozoospermia | Feingold Syndrome | Hyperuricemic Nephropathy, Familial Juvenile | Dystonia Musculorum Deformans | Hyperlipidemia | Hypertension | WAGR Syndrome | Gynecomastia | Fibronectin Glomerulopathy | Cardiospondylocarpofacial Syndrome | Double Outlet Right Ventricle | Werner's Syndrome | Posterior Polar Cataract | NGLY1 Deficiency | COACH Syndrome | Familial Digital Arthropathy-brachydactyly | GNE Myopathy | Osteogenesis Imperfecta Type VI | Thyroiditis | Evans Syndrome | Hereditary Pyropoikilocytosis | Saul-Wilson Syndrome | Wagner Disease | Hemorrhagic Disorders | Overactive Bladder | Transient Bullous Dermolysis Of The Newborn | Torticollis | Sengers Syndrome | Hypotension, Orthostatic | Exotropia | Harlequin Ichthyosis | Antithrombin III Deficiency | Homocystinuria | Holt-Oram Syndrome | Behavioral Variant Of Frontotemporal Dementia | Megaloblastic Anemia | Carotid Artery Disease | Glutathione Synthetase Deficiency | Gigantism | Axenfeld-Rieger Syndrome | Anuria | Primary Familial Brain Calcification | Stroke, Ischemic | Hereditary Spastic Paraplegia | Antisynthetase Syndrome | Hyperinsulinism-hyperammonemia Syndrome | Hepatic Steatosis | Cranioectodermal Dysplasia | Brachydactyly | Dysfibrinogenemia | Epilepsy | Molybdenum Cofactor Deficiency | Nance-Horan Syndrome | Analgesia | Speech Disorders | Cervicitis | Beckwith-Wiedemann Syndrome | Thyroid Hormone Resistance | Keratitis | Leprosy | Vitamin K Deficiency | Basal Ganglia Cerebrovascular Disease | Lymphangiomatosis | Splenomegaly | Carcinoma In Situ | Hernia, Inguinal | GATA2 Deficiency | Systemic Mastocytosis | Panuveitis | Malaria, Cerebral | Hypertension, Essential | Chromosome 5q Deletion Syndrome | Acne Vulgaris | Swine Influenza | Platelet Disorders | Williams Syndrome | Specific Granule Deficiency | Hyperacusis | Skin Fragility-woolly Hair Syndrome | Coloboma | Erythrokeratodermia Variabilis | Pulmonary Sclerosing Hemangioma | Pyruvate Carboxylase Deficiency Disease | Syncope | Retinopathy Of Prematurity | Diabetes Type 1 | 3-methylglutaconic Aciduria | Cholestasis, Intrahepatic | Plasmacytoma | Growth Hormone Excess | Thanatophoric Dysplasia Type 1 | Parapsoriasis | MIRAGE Syndrome | Jacobsen Syndrome | Cancer, Colon