Pain
About the Disease
Paine Syndrome, also known as pain disorder, is related to paroxysmal extreme pain disorder and indifference to pain, congenital, autosomal recessive. An important gene associated with Paine Syndrome is HFE (Homeostatic Iron Regulator), and among its related pathways/superpathways are Cardiac conduction and Neuropathic Pain-Signaling in Dorsal Horn Neurons. The drugs Pregabalin and Dinoprostone have been mentioned in the context of this disorder. Affiliated tissues include dorsal root ganglion, spinal cord and breast, and related phenotypes are microcephaly and spastic diplegia
Common Targets / Biomarkers
P32835 | G4543 | G84876 | G2864 | G1902 | G4804 | G2557 | G8514 | G187 | G4914 | G2902 | P11019 | G151 | G4217 | G10021 | G2897 | G1859 | G7498 | Phosphodiesterase 1 (PDE1) (nonspecified subtype) | G3786 | G5733 | G1803 | G2741 | G10846 | DNA-Directed RNA Polymerase (nonspecified subtype) | G136 | G1610 | G1020 | G902 | G2905 | G3290 | G1520 | G7157 | G2643 | G5739 | G6532 | G3814 | G729230 | G2288 | G759 | G5321 | G2932 | G1139 | G5979 | G7015 | G7224 | G3356 | G836 | G9132 | CDK5/p25 | Voltage-gated K(v) channel (nonspecified subtype) | G6768 | G5770 | P42190 | Somatostatin receptor (nonspecified subtype) | Tachykinin Receptor (nonspecified subtype) | G2561 | G11188 | Tyrosine Kinase (nonspecified subtype) | G8913 | G3274 | Neurotrophic Factor (nonspecified subtype) | G590 | G6328 | Phospholipase A2 (nonspecified subtype) | G4321 | G231 | G5467 | G3360 | G4313 | Acetylcholine Receptors (Nicotinic) (nAChR) (nonspecified subtype) | P32844 | G64866 | Cyclin-dependent kinase (nonspecified subtype) | G2159 | C-X-C Chemokine Receptor CXCR1/CXCR2 (IL-8 Receptor) (nonspecified subtype) | G6697 | G5481 | Endothelin-Converting Enzymes (ECE) (nonspecified subtype) | P6463 | G4886 | G5024 | Protein Tyrosine Phosphatase (PTP) (nonspecified subtype) | G1/S-specific cyclin-E (nonspecified subtype) | G387129 | G2832 | G1025 | G29881 | P16704 | CDK9/Cyclin T1 | Thyroid hormone receptor (nonspecified subtype) | G887 | G6334 | Mitogen-Activated Protein Kinase (MAP Kinase)-Activated Protein Kinase (nonspecified subtype) | Acid-Sensing Ion Channel (ASIC) (nonspecified subtype) | P32845 | G2357 | Glutamate Transporter (nonspecified subtype) | G116085 | P6348 | G338567 | alpha-Adrenoceptor (nonspecified subtype) | G771 | G4916 | G1514 | G775 | G255738 | G6446 | G3717 | G8856 | G5600 | G1621 | G4985 | Steroid 5-alpha-Reductase (nonspecified subtype) | G8654 | G3061 | G6677 | G409 | Opioid receptor (nonspecified subtype) | G3783 | G4015 | G5156 | G8569 | G55107 | Mitogen-Activated Protein Kinase (nonspecified subtype) | G2151 | G5020 | G6098 | G3815 | G2912 | cGMP-Dependent Protein Kinase (nonspecified subtype) | Kir 3.1/3.4 | G27436 | G6272 | G6753 | G1808 | G150 | G54106 | G4137 | G2841 | LanC-like proteins (nonspecified subtype) | G3776 | G2906 | G995 | G7412 | G1236 | P16176 | G2916 | G2950 | G4296 | Casein kinase I (nonspecified subtype) | G3747 | G2903 | G3577 | G1958 | G9020 | G9446 | G6536 | Peroxisome Proliferator-Activated Receptors (PPAR) (nonspecified subtype) | G4544 | G51135 | G3458 | Gap junction Connexin ( (nonspecified subtype) | G6550 | G2166 | G4887 | G5595 | G5894 | G protein-Coupled Inwardly-Rectifying Potassium Channel (GIRK) (nonspecified subtype) | G2316 | G8989 | P16556 | G140 | G7099 | G4843 | P19243 | G6329 | G3689 | Raf kinase (nonspecified subtype) | G185 | G2891 | G673 | G2898 | G3716 | G1131 | Histone acetyltransferase (HAT) (nonspecified subtype) | G3718 | G1816 | G9356 | G3558 | P5833 | G155 | G904 | G114548 | G3552 | G153 | G7517 | G3702 | Chloride channel (nonspecified subtype) | G706 | G51185 | Phospholipase C (nonspecified subtype) | G1812 | G100 | G5734 | G25976 | G9780 | G5753 | P16964 | G7329 | G7428 | G4987 | G408 | G1903 | G2917 | G6510 | Adenylate Cyclase (nonspecified subtype) | G5031 | G3741 | Histone deacetylase (nonspecified subtype) | G3375 | P12578 | G3588 | G10110 | P11113 | G154 | G9261 | G59283 | G4311 | G472 | G2837 | P16740 | G2194 | G9064 | Interferon (nonspecified subtype) | Adenosine deaminase (nonspecified subtype) | Potassium/Sodium Hyperpolarization-Activated Cyclic Nucleotide-Gated Channel (nonspecified subtype) | G55584 | 15-Lipoxygenase (nonspecified subtype) | CDK8/Cyclin C | G2828 | G7113 | G7225 | G3269 | G3748 | G24145 | Neurotrophic Tyrosine Kinase Receptor (TRK) (nonspecified subtype) | Dimethylargininase (nonspecified subtype) | G4159 | G2739 | G1393 | Na+/K+-ATPase (nonspecified subtype) | G2289 | G2554 | G2562 | P34664 | G3753 | G9475 | G11280 | G6335 | beta-Adrenoceptor (nonspecified subtype) | G2892 | Phosphatidylinositol 4-Kinase beta (PI4K-beta) (nonspecified subtype) | Kir 3.1/3.2 | P5867 | Neuropeptide FF Receptor (nonspecified subtype) | G6754 | G54207 | G9448 | G3361 | G50508 | G2548 | G4316 | G9376 | Trypsin (nonspecified subtype) | Vascular endothelial growth factor receptor (VEGFR) (nonspecified subtype) | G23620 | G57468 | Serine protease (nonspecified subtype) | G2798 | G11251 | P13475 | KCNQ Channels (K(v) 7) (nonspecified subtype) | G5025 | G23576 | G5327 | G1080 | Heme Oxygenase (HO) (nonspecified subtype) | G3760 | G4322 | G3062 | G5133 | G3576 | G760 | G2170 | G22848 | Mu/delta-Opioid receptor heterodimer (MDOR) | L-Type calcium channel (nonspecified subtype) | Prostanoid TP receptor (nonspecified subtype) | Inhibitory kappaB Kinase (IKK) (nonspecified subtype) | P11025 | G6323 | G823 | G5476 | P5662 | G1786 | G898 | CDK1/Cyclin B | G3784 | G196743 | G796 | G5729 | G27159 | Caspase (nonspecified subtype) | G6869 | G2145 | G25 | G1588 | G4889 | G23621 | G3094 | G6750 | G4067 | G79823 | G2517 | G5292 | G10203 | G5888 | G4035 | G57406 | G57626 | G3579 | Arrestin (nonspecified subtype) | G6885 | G4350 | G2171 | G5138 | alpha1-Adrenoceptor (nonspecified subtype) | G1742 | G53831 | sigma Receptor (nonspecified subtype) | G2346 | G104909134 | Phospholipase A2, Cytosolic (nonspecified subtype) | G3362 | G1394 | Orexin receptor (nonspecified subtype) | G412 | G216 | G3358 | Dopamine receptor (nonspecified subtype) | Nitric oxide synthase (NOS) (nonspecified subtype) | G6538 | Poly [ADP-ribose] polymerase (nonspecified subtype) | Potassium Channels (nonspecified subtype) | HTR1B | G1136 | G4923 | G10598 | G9783 | G4282 | G2918 | G5605 | G610 | G2358 | G9290 | G2899 | G6531 | Muscarinic Acetylcholine Receptor (mAChR) (nonspecified subtype) | P24924 | CDK2/Cyclin A | G4129 | G22806 | 5-Hydroxytryptamine Receptor 2 (5-HT2) (nonspecified subtype) | G57007 | P33507 | P42991 | G162514 | G53637 | Sterol O-acyltransferase (ACAT) (nonspecified subtype) | G3762 | G1814 | G5147 | G369 | G177 | G7166 | G2740 | G55 | G114 | G8001 | G2519 | G2558 | G146 | G27346 | G6331 | G240 | G7415 | G2263 | G4988 | G10008 | G6774 | G5243 | G5294 | G10135 | G6999 | G186 | G7515 | G768 | G5159 | Cyclooxygenase (COX) (nonspecified subtype) | G773 | G5027 | P2X Receptor (nonspecified subtype) | G340061 | Cannabinoid receptor (nonspecified subtype) | G6732 | G1436 | G79837 | G2913 | G10886 | P6321 | G1636 | G4160 | G238 | G283871 | G9520 | G728 | Gastric H+/K+-ATPase | G5602 | G117 | G1719 | G2146 | G3146 | Adenosine receptor (nonspecified subtype) | Leukotriene B4 receptor (LTB4-R) (nonspecified subtype) | P5859 | G2173 | G5066 | G23704 | G2534 | G2911 | G623 | G7123 | G4363 | G10320 | G11103 | G1513 | G51305 | G3291 | G6755 | G7226 | NADPH Oxidase (nonspecified subtype) | G1901 | G10919 | G57582 | G5328 | Large Conductance BK(Ca) Potassium Channel (Maxi K+ Channel) (nonspecified subtype) | G1133 | G41 | G5021 | G8737 | Carboxypeptidase A (nonspecified subtype) | G6529 | G3818 | G695 | G1956 | G2081 | Tryptase (nonspecified subtype) | G1269 | G2904 | Cytochrome P450 Enzymes (nonspecified subtype) | G7124 | G10013 | G54822 | G5588 | G10887 | Voltage-Gated Calcium Channel alpha-2/delta (nonspecified subtype) | G886 | G983 | High affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7 (nonspecified protein) | G26279 | G3162 | P10999 | G2984 | G4312 | G22953 | G2563 | G1508 | G993 | Glutaminase (nonspecified subtype) | G3763 | G10369 | Cyclin A (nonspecified subtype) | Rho kinase (ROCK) (nonspecified subtype) | G7048 | G4780 | G4881 | G9992 | G1889 | G27035 | G5468 | G29909 | G5731 | Phospholipase A2, Secretory (sPLA2) (nonspecified subtype) | Aggrecanase (nonspecified subtype) | G7941 | 5-Hydroxytryptamine Receptor (nonspecified subtype) | G57105 | Gap Junction Protein (nonspecified subtype) | G595 | G2555 | G10000 | G9002 | G3654 | cGMP-inhibited 3',5'-cyclic phosphodiesterase 3 (PDE3) (nonspecified subtype) | G4602 | G545 | G64106 | Mitogen-activated protein kinase p38 (MAPK p38) (nonspecified subtype) | G1813 | G7443 | CDK2/Cyclin E | G2908 | G1129 | Sarcoplasmic/Endoplasmic Reticulum Calcium ATPase (SERCA) (nonspecified subtype) | G5290 | P32669 | G3756 | G6647 | G3620 | G3790 | G6540 | Protein Tyrosine Phosphatase Type IVA (nonspecified subtype) | G1141 | G1240 | Cyclin-dependent kinase inhibitor (nonspecified subtype) | G4915 | Phosphodiesterase IV (PDE4) (nonspecified subtype) | G747 | Phosphodiesterase 8 (nonspecified subtype) | G1545 | G6578 | G4790 | Retinoid RXR receptor (nonspecified subtype) | G4142 | G710 | G5144 | G1137 | Calcium-activated chloride channel regulators (nonspecified subtype) | G3736 | G6714 | G4986 | G2914 | G5743 | G3557 | G2069 | G3569 | P40377 | G2831 | G1022 | G290 | G1806 | P16191 | G627 | Dual Specificity Mitogen-Activated Protein Kinase Kinase (MEK) (nonspecified subtype) | P6747 | G4048 | G799 | G5581 | CDK7/Cyclin H | G6790 | G2258 | G777 | G11255 | G1268 | G1909 | G5406 | G5465 | Superoxide dismutase (SOD) (nonspecified subtype) | Phosphodiesterase (nonspecified subtype) | G8639 | G27163 | G1524 | G5972 | G4056 | G2030 | G1017 | G117194 | P32821 | alpha-Amylase (nonspecified subtype) | G147 | Calcium channel (nonspecified subtype) | G7442 | G10495 | G5724 | G3363 | G59340 | G18 | G6097 | G4803 | G10733 | G348980 | G4157 | G43 | G8973 | G5592 | G134864 | Mitogen-activated protein kinase (JNK) (nonspecified subtype) | G3785 | P34550 | G152 | G246 | G107 | G5732 | Neurotensin receptor (nonspecified subtype) | P16683 | G1312 | G3765 | P6884 | G9311 | 5-Hydroxytryptamine Receptor 3 (5-HT3 receptor) (nonspecified subtype) | G7297 | G51056 | G6326 | G1395 | G142 | Heat shock protein 90 (nonspecified subtype) | G79054 | G8911 | G120892 | G3780 | G6622 | G2847 | G5598 | G2559 | G3065 | G3949 | G3791 | G9048 | Protein kinase C (nonspecified subtype) | G5168 | G5293 | G5737 | G7150 | G26986 | G3352 | Phosphatidylinositol 3-kinase (PI3K) (nonspecified subtype) | P9058 | G552 | G5742 | G3350 | G3630 | P5767 | G6530 | G8811 | P16192 | P32822 | G4882 | G6336 | G6916 | G6524 | G3553 | G151306 | P6320 | G2353 | G105378917 | Glutamate Receptor Ionotropic (nonspecified subtype) | G4128 | G23476 | G2556 | G3684 | Carbonic Anhydrase (nonspecified subtype) | G221955 | G2587 | G9429 | G4233 | Inward Rectifier Potassium Channel (nonspecified subtype) | Melanocortin receptor (nonspecified subtype) | Monoamine oxidase (MAO) (nonspecified subtype) | G774 | G3708 | G7421 | G7525 | G5142 | P18508 | G1501 | G727 | Alpha-2 Adrenergic receptors (nonspecified subtype) | G2053 | G5320 | G8912 | G1445 | G56923 | Inward Rectifier Potassium Channel (nonspecified subtype) | Bradykinin receptor (nonspecified subtype) | G3745 | G6870 | G2100 | G9152 | G9718 | G327 | G3992 | G7852 | P36529 | P32823 | Sodium channel (nonspecified subtype) | G4921 | G84634 | G2915 | P40594 | G6752 | G2281 | G1134 | G1454 | G2280 | G2565 | G2859 | G624 | G11040 | Cyclin B (nonspecified subtype) | G1509 | G6571 | G4318 | Ectonucleoside triphosphate diphosphohydrolase (nonspecified subtype) | G148 | G2931 | Tyrosine-Protein Kinases Src (nonspecified subtype) | G7276 | G781 | G3738 | G10280 | G7184 | G2150 | G23411 | G5604 | P32831 | G3751 | Prostanoid Receptor (nonspecified subtype) | G217 | G2560 | Epoxide Hydrolase (nonspecified subtype) | P6176 | G1432 | G1128 | G8317 | G10320 | G3156 | G3586 | CCK receptor (nonspecified subtype) | G6865 | G558 | G1132 | G140733 | G4314 | G7299 | G57121 | Kainate Receptor (GluR) (nonspecified subtype) | G9536 | Lipoxygenase (nonspecified subtype) | G6093 | G128674 | G134 | G2688 | P10238 | P2X2/3 Receptor Complex | G2872 | G7223 | G9463 | G132 | Metabotropic glutamate (mGluR) receptor (nonspecified subtype) | G4842 | P16092 | G139760 | G3782 | P6058 | G6778 | G4049 | G2322 | G5291 | G3357 | G135 | Calpain (nonspecified subtype) | G1815 | G8841 | G3383 | G124274 | Interleukin-1 (nonspecified subtype) | DNA Topoisomerase II (nonspecified subtype) | G8078 | G116511 | G7014 | G259249 | G3746 | G51393 | G9254 | G3752 | Lysophospholipid (edg) Receptors (nonspecified subtype) | G2566 | G2597 | cAMP Phosphodiesterase (nonspecified subtype) | G11343 | G59341 | G3355 | G116 | Prostaglandin EP Receptor (nonspecified subtype) | G2147 | G5023
Other Diseases
Palmoplantar Keratoderma | Palsy, Cerebral | Pancreatitis | Pancreatitis, Chronic | Pancytopenia | Panic Disorder | Panniculitis | Pantothenate Kinase-associated Neurodegeneration | Panuveitis | Papilledema | Papilloma | Papillon-Lefevre Syndrome | Papillorenal Syndrome | Papulopustular Rosacea | Paraganglioma | Paraplegia | Parapsoriasis | Parkinson Disease 6, Autosomal Recessive Early-onset | Parkinson's Disease | Parkinsonism | Paronychia | Paroxysmal Kinesigenic Dyskinesia | Paroxysmal Nocturnal Hemoglobinuria | Partington Syndrome | Parvovirus B19 Infection | PASLI Disease | Patent Ductus Arteriosus | Patent Foramen Ovale | Paternal Uniparental Disomy Of Chromosome 14 | Pathological Gambling | Pearson Syndrome | Peeling Skin Syndrome Type B | Peeling Skin Syndrome, Acral Type | Pelizaeus-Merzbacher Disease | Pelvic Inflammatory Disease | Pemphigoid | Pemphigus | Pemphigus Foliaceus | Pemphigus Vulgaris | Pendred Syndrome | Pericarditis | Periodic Limb Movement Disorder | Periodontitis | Peripheral Neuropathy | Peripheral T-cell Lymphoma | Peritonitis | Perivascular Epithelioid Cell Tumor | Periventricular Leukomalacia | Periventricular Nodular Heterotopia | Pernicious Anemia | Peroxisomal Disorder | Persistent Fetal Circulation | Persistent Hyperplastic Primary Vitreous | Persistent Mullerian Duct Syndrome | Persistent Truncus Arteriosus | Personality Disorders | Peters-plus Syndrome | Peutz-Jeghers Syndrome | Peyronie's Disease | Pfeiffer Syndrome | PHARC Syndrome | Phenylketonuria | Phenylketonuria II | Pheochromocytoma | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Phosphoglycerate Dehydrogenase Deficiency | Photosensitivity | Pierpont Syndrome | Pierre Robin Syndrome | Pierson Syndrome | Pigment Dispersion Syndrome | Pilomatrix Carcinoma | Pineoblastoma | Pitt-Hopkins Syndrome | Pituitary Disorders | Pituitary Dwarfism | Pituitary Stalk Interruption Syndrome | Placenta Previa | Plasma Cell Dyscrasia | Plasma Cell Leukemia | Plasmacytoma | Platelet Disorders | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Pleomorphic Xanthoastrocytoma | Pleural Tuberculosis | Pleurisy | Pneumococcal Meningitis | Pneumoconiosis | Pneumonia, Bacterial | Pneumonia, Mycoplasma | Pneumonia, Viral | Pneumothorax | POEMS Syndrome | Poikiloderma With Neutropenia | Poirier-Bienvenu Neurodevelopmental Syndrome | Polyarteritis Nodosa | Polycystic Kidney, Autosomal Dominant | Polycystic Kidney, Autosomal Recessive | Polycystic Liver | Polycystic Ovary Syndrome | Polycythemia | Polycythemia Vera | Polydactyly | Polymicrogyria | Polymyalgia Rheumatica | Polymyositis | Polyneuropathy | Polyomavirus Nephropathy | Polyradiculopathy | Pompe Disease | Pontocerebellar Hypoplasia | Pontocerebellar Hypoplasia Type 2 | Porencephaly | Poretti-Boltshauser Syndrome | Porokeratosis | Porphyria | Porphyria Cutanea Tarda | Porphyria, Acute Intermittent | Porphyria, Variegate | Portal Vein Thrombosis | Postaxial Polydactyly | Posterior Polar Cataract | Postpartum Depression | Postpoliomyelitis Syndrome | Potocki-Shaffer Syndrome | Pouchitis | Prader-Willi Syndrome | Pre-eclampsia | Preaxial Polydactyly | Precocious Puberty | Prediabetes | Pregnancy, Ectopic | Premature Ejaculation | Premenstrual Syndrome | Presbycusis | Presbyopia | Priapism | Primary Aldosteronism | Primary Biliary Cholangitis | Primary Carnitine Deficiency | Primary Cutaneous Amyloidosis | Primary Erythromelalgia | Primary Familial Brain Calcification | Primary Hyperoxaluria | Primary Hyperoxaluria Type 1 | Primary Hyperoxaluria Type 3 | Primary Lateral Sclerosis | Primary Ovarian Insufficiency | Primary Pigmented Nodular Adrenocortical Disease | Primary Progressive Aphasia | Primary Progressive Nonfluent Aphasia | Primary Sclerosing Cholangitis | Primary Torsion Dystonia | Primrose Syndrome | Proctitis | Progressive Encephalopathy-optic Atrophy Syndrome | Progressive External Ophthalmoplegia | Progressive Familial Intrahepatic Cholestasis | Progressive Familial Intrahepatic Cholestasis Type 1 | Progressive Familial Intrahepatic Cholestasis Type 2 | Progressive Familial Intrahepatic Cholestasis Type 3 | Progressive Myoclonic Epilepsy | Progressive Osseous Heteroplasia | Prolactinoma | Prolidase Deficiency | Prolymphocytic Leukemia | Proopiomelanocortin Deficiency | Prostatitis | Proteasome-associated Autoinflammatory Syndrome 2 | Protein C Deficiency | Protein S Deficiency | Proximal Symphalangism | Prune Belly Syndrome | Prurigo Nodularis | Pseudo-pseudohypoparathyroidism | Pseudoachondroplasia | Pseudoexfoliation Syndrome | Pseudohermaphroditism | Pseudohypoaldosteronism | Pseudohypoparathyroidism Type 1A | Pseudohypoparathyroidism Type 1B | Pseudohypoparathyroidism Type 1C | Pseudohypoparathyroidism Type 2 | Pseudomyxoma Peritonei | Psoriasis | Pterygium | Pulmonary Alveolar Microlithiasis | Pulmonary Alveolar Proteinosis | Pulmonary Capillary Hemangiomatosis | Pulmonary Sclerosing Hemangioma | Pulmonary Stenosis | Pulmonary Tuberculosis | Pulmonary Vein Stenosis | Pulmonary Veno-occlusive Disease | Pulverulent Zonular Cataract | Pupil Disorders | Pure Autonomic Failure | Pure Red Cell Aplasia | Purpura | Purpura, Thrombotic Thrombocytopenic | Pycnodysostosis | Pyelonephritis | Pyloric Stenosis, Infantile Hypertrophic | Pyoderma Gangrenosum | Pyruvate Carboxylase Deficiency Disease | Pyruvate Decarboxylase Deficiency | Pyruvate Dehydrogenase Deficiency | Pyruvate Kinase Deficiency | Raine Syndrome | Rash | Raynaud Phenomenon | Recurrent Respiratory Papillomatosis | Reflex Epilepsy | Relapsing Polychondritis | REM Sleep Behavior Disorder | Renal Dysplasia | Renal Failure | Renal Hypomagnesemia 3 | Renal Hypouricemia | Renal Medullary Carcinoma | Renal Oncocytoma | Renal Tubular Acidosis | Renal Tubular Dysgenesis | Renal-hepatic-pancreatic Dysplasia | Renpenning Syndrome | Restless Legs Syndrome | Restrictive Dermopathy | Reticular Dysgenesis | Retinal Coloboma | Retinal Degeneration | Retinal Detachment | Retinal Diseases | Retinal Dystrophy | Retinal Telangiectasia | Retinal Vasculitis | Retinitis | Retinitis Pigmentosa | Retinitis Pigmentosa 3 | Retinoblastoma | Retinopathy Of Prematurity | Retinopathy, Diabetic | Retinoschisis | Rett Syndrome | Reye Syndrome | Rhabdoid Tumor | Rhabdomyosarcoma | Rhabdomyosarcoma, Alveolar | Rhabdomyosarcoma, Embryonal | Rheumatic Heart Disease | Rheumatoid Arthritis | Rhinitis | Rhizomelic Chondrodysplasia Punctata | Riboflavin Transporter Deficiency Neuronopathy | Richter's Syndrome | Rickets | Rift Valley Fever | Roberts Syndrome | Robinow Syndrome | Rolandic Epilepsy | Rosacea | Rothmund-Thomson Syndrome | Rotor Syndrome | Rubeosis Iridis | Rubinstein-Taybi Syndrome | Saethre-Chotzen Syndrome | Salla Disease | Sandhoff Disease | SAPHO Syndrome | Sarcoidosis | Sarcoidosis, Pulmonary | Sarcoma | Sarcoma, Alveolar Soft Part | Sarcoma, Endometrial Stromal | Sarcoma, Ewing | Sarcomatoid Carcinoma Of The Lung | Sarcosinemia | Saul-Wilson Syndrome | Scabies | Scapuloperoneal Myopathy, X-linked Dominant | Scapuloperoneal Spinal Muscular Atrophy | Schaaf-Yang Syndrome | Schamberg Disease | Schindler Disease | Schistosomiasis | Schistosomiasis Mansoni | Schizencephaly | Schizophrenia | Schizotypal Personality Disorder | Schnitzler Syndrome | Schnyder Crystalline Corneal Dystrophy | Schuurs-Hoeijmakers Syndrome | Schwannoma | Schwannomatosis | Schwartz-Jampel-Aberfeld Syndrome | Scleritis | Sclerocornea | Scleroderma | Scleroderma, Diffuse | Sclerosing Cholangitis | Sclerosteosis | Sclerosteosis 2 | Scoliosis | Seasonal Mood Disorder | Seborrheic Dermatitis | Seizures | Seizures-scoliosis-macrocephaly Syndrome | Seminoma | Sengers Syndrome | Senior-Loken Syndrome | Sensorineural Hearing Loss | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Sensory Neuropathy | Sepiapterin Reductase Deficiency | Sertoli Cell-only Syndrome | Sezary Syndrome | Shock, Cardiogenic | Short-chain Acyl-CoA Dehydrogenase Deficiency | Shprintzen-Goldberg Syndrome | Shwachman-Bodian-Diamond Syndrome | Sialoadenitis | Sick Sinus Syndrome | Sick Sinus Syndrome 1 | Sickle Cell Anemia | Sickle Cell Disease | Silicosis | Silver-Russell Syndrome | Sitosterolemia | Situs Inversus | Sjogren Syndrome | Skin Carcinoma | Skin Fragility-woolly Hair Syndrome | Skin Papilloma | Sleep Apnea | Sleep Apnea, Central | Sleep Apnea, Obstructive | Sleep Disorder | Small Lymphocytic Lymphoma | Smith-Kingsmore Syndrome | Smith-Lemli-Opitz Syndrome | Smith-Magenis Syndrome | Smoldering Myeloma | Snyder-Robinson Syndrome | Sorsby Fundus Dystrophy | Sotos Syndrome | Spastic Paraplegia Type 7 | Spasticity | Specific Granule Deficiency | Speech Disorders | Spina Bifida | Spinal And Bulbar Muscular Atrophy | Spinal Cord Diseases | Spinal Muscular Atrophy | Spinal Muscular Atrophy Type 2 | Spinal Muscular Atrophy Type 3 | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Spinocerebellar Ataxia Type 1 | Spinocerebellar Ataxia Type 10 | Spinocerebellar Ataxia Type 12 | Spinocerebellar Ataxia Type 13 | Spinocerebellar Ataxia Type 14 | Spinocerebellar Ataxia Type 15 | Spinocerebellar Ataxia Type 16 | Spinocerebellar Ataxia Type 17 | Spinocerebellar Ataxia Type 2 | Spinocerebellar Ataxia Type 20 | Spinocerebellar Ataxia Type 21 | Spinocerebellar Ataxia Type 23 | Spinocerebellar Ataxia Type 27 | Spinocerebellar Ataxia Type 28 | Spinocerebellar Ataxia Type 3 | Spinocerebellar Ataxia Type 31 | Spinocerebellar Ataxia Type 38 | Spinocerebellar Ataxia Type 40 | Spinocerebellar Ataxia Type 42 | Spinocerebellar Ataxia Type 5 | Spinocerebellar Ataxia Type 6 | Spinocerebellar Ataxia Type 7 | Spinocerebellar Ataxia Type 8 | Spitz Nevus | Spitzoid Melanoma | Splenomegaly | Split Hand-foot Malformation | Sponastrime Dysplasia | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Spondylo-ocular Syndrome | Spondyloarthritis | Spondylocarpotarsal Synostosis Syndrome | Spondylocostal Dysostosis | Spondyloepiphyseal Dysplasia Tarda, X-linked | Spondylolisthesis | Spondylometaphyseal Dysplasia | Spondyloperipheral Dysplasia | Spondylosis | Sporadic Hemiplegic Migraine | Sporadic Inclusion Body Myositis | Stargardt Disease | Steel Syndrome | Stevens-Johnson Syndrome | Stickler Syndrome | Stiff-man Syndrome
