Disease

Autism Spectrum Disorders

About the Disease
Autism Spectrum Disorder, also known as autism spectrum disorders, is related to autism and attention deficit-hyperactivity disorder, and has symptoms including widespread abnormalities of social interactions, severely restricted interests and highly repetitive behavior. An important gene associated with Autism Spectrum Disorder is SHANK2 (SH3 And Multiple Ankyrin Repeat Domains 2), and among its related pathways/superpathways are Thyroid hormones production and peripheral downstream signaling effects and Rett syndrome causing genes. The drugs Acetylcholine and Dexmedetomidine have been mentioned in the context of this disorder. Affiliated tissues include eye, brain and prefrontal cortex, and related phenotypes are nervous system and growth/size/body region

Common Targets
GPR139 | MAP2K6 | HTRA4 | ODF2 | ZRANB3 | HTR1A | PIK3R5 | RBFOX1 | TMEM132C | SLC22A14 | CDC42EP1 | CLEC7A | AKAP9 | CD74 | RALYL | ACHE | COL6A5 | SHANK3 | MKNK2 | C1S | MED13 | CNGA3 | G1432 | RETREG1 | G4233 | RNF135 | AARS1 | KIAA1549L | PRPS2 | EN2 | NOS1 | GTF2F2 | VDR | NEO1 | SPTLC2 | Metabotropic glutamate (mGluR) receptor (nonspecified subtype) | GABA(A) receptor | MTCL1 | TRIM2 | SSBP3 | MEGF11 | PIK3CB | CSNK1G1 | GLRA2 | DRD4 | Voltage-Gated Sodium Channel Complex | TYW1B | TNPO3 | mTOR complex 1 | G3569 | ITPR3 | SCFD2 | EPB41 | ADNP | GNAL | WNT3A | SIGMAR1 | Gamma-Aminobutyric acid type B receptor | SLC12A3 | LIMK1 | GRIN1 | PTPN7 | HSD17B11 | PLA2G4A | THSD4 | UBR5 | TMCO4 | KCNQ4 | CAMK4 | SHC4 | T-Type Calcium Channel | AEBP2 | ZNF148 | MYT1L | PLCZ1 | NLGN3 | KCNQ3 | Sodium channel (nonspecified subtype) | MAP3K9 | LINC02398 | DAB1 | SAMD12 | LRRC24 | ABCA7 | NYNRIN | HTR2B | SCN3A | EPB41L1 | TRPC5 | ASPM | INVS | ABCC12 | ESPNL | ITIH3 | TCF12 | GABRG2 | CDKN2B-AS1 | GNAO1 | PRKCZ | DYNC1H1 | DIP2C | TRPV2 | PAX2 | ATP1B4 | AVPR1B | RNF130 | BANP | TMBIM6 | TRIP12 | MIR137 | G7124 | CARD11 | GFAP | FAM13A | CACNA1G | GPR52 | CAMSAP3 | IVD | IL1B | DYRK1A | KDM4C | CPNE7 | TAF1 | BUB1B | SLC35A3 | CMIP | IRS2 | PIGL | ZPBP | BAZ1A | NWD2 | AQP4 | DPP4 | GABRB2 | RAB11B | CDKL5 | TLN2 | CDKAL1 | LINC02055 | LRP5 | PDE10A | HLA-G | TMEM132B | G3480 | CCKBR | GRIA1 | ZEB2 | TMCC2 | WDR1 | NEDD4L | NIPA2 | CMPK2 | RASGRP1 | FANK1 | DPYSL2 | UBE2D2 | ANKK1 | ABCA9 | HLA-DQB2 | WWP1 | TNC | SCLT1 | CCDC171 | SERPINB13 | TSC2 | CALM1 | ARMC9 | ADCY3 | DDX11 | RASGEF1A | LINC01508 | TP53I3 | PTPN12 | SCN8A | ATP1B1 | CAMTA1 | PTPN1 | CNTNAP5 | SHANK2 | CACNA1C | GTF3C2 | Glutamate Transporter (nonspecified subtype) | LPP | ZHX2 | ASXL3 | ABCA8 | DUSP22 | ADTRP | ROS1 | TCF4 | TM2D1 | MKNK1 | CHRNA7 | CHODL | MGRN1 | MMS22L | AVPR2 | GSK3B | EGFEM1P | GOLM2 | IL12RB1 | PRR21 | DLX6-AS1 | BCHE | SYNE3 | NHS | IMMP2L | PAPPA2 | TCEANC | CACNB2 | NRG2 | PRICKLE2 | BCAS1 | ALLC | NSMCE1 | PPP2R5C | PRKD1 | KCTD16 | PCMTD1 | DNA2 | TCF20 | MECP2 | JMJD1C | OXT | PHF21A | NCKAP1 | CHD2 | RASGRF2 | G protein-Coupled Inwardly-Rectifying Potassium Channel (GIRK) (nonspecified subtype) | TAFA1 | ENPP3 | GRM2 | TRPM1 | ERCC2 | PDGFD | PRTG | CTLA4 | ADRA2A | ZNF496 | NAV1 | SORCS3 | VPS8 | NTM | WDR47 | CUL4B | DYNC1LI2 | SLAIN1 | VPS18 | SEZ6L | Fibroblast growth factor (FGF) (nonspecified subtype) | SEC23A | FOXP1 | GUCY1A2 | LUZP2 | FAM186A | AGMAT | TRIP10 | RYR2 | CYP2E1 | BST1 | FGA | AFG1L | NUDT9 | RCAN2 | MAN1A2 | IL3RA | SLC6A4 | CLASP1 | DDI2 | HTR2A | SORCS1 | PLCE1 | WAC | ASH1L | SS18L1 | FAM47A | TF | ELK4 | TNNI3K | HMGN3 | WWP2 | COL5A1 | ACSL4 | GBE1 | SLC19A1 | POGZ | CPAMD8 | NHSL2 | NSD1 | TAF6 | OPRL1 | PRKAG2 | CNTN6 | CELF5 | ATXN3 | TIAM1 | AGBL1 | NF-kappaB (NFkB) | GRIN2A | CIT | PCDH15 | BBS12 | ADA | NLGN4X | UPF3B | DYTN | PSD3 | MAPKAPK2 | RIT2 | PYGO1 | KIF2A | ZFP1 | EPHA3 | CLN8 | PDGFRA | GLO1 | NAV2 | GPR142 | EXOC7 | MOB3B | NRN1 | DGUOK | KCNK10 | GRIA3 | ATP5MJ | MEF2C | MCPH1 | LINC01484 | LRFN1 | PAX5 | GABRG3 | NEDD4 | FANCL | SLC22A8 | DCX (DDB1-CUL4-X-box) E3 protein ligase complex | GPR153 | IFNLR1 | SLC12A5 | IFNG | RORA | ZNF480 | NMDA receptor | TRPC6 | NDRG1 | OR52L1 | 15-Lipoxygenase (nonspecified subtype) | MGAT5B | FAAH | ATP2B1 | IFT88 | AADACL2-AS1 | TRPA1 | SNRNP35 | MARCKS | NOS2 | RGCC | KMT2A | SPATA13 | NAA10 | FGGY | MAP3K13 | MAP4K4 | POLR3D | DRD1 | TBC1D14 | WDR7 | CHST7 | NF1 | CYP2S1 | POU6F2 | Eukaryotic Translation Initiation Factor 4A (eIF-4A) | CCDC18 | KIT | SMARCC2 | UBE3A | G672 | GALNTL5 | DDR1 | UBE2J1 | GABRA1 | PPP2R5D | GSTM1 | mTOR complex 2 | CAMK2A | Glycogen synthase kinase 3 (GSK-3) (nonspecified subtype) | ERBB4 | GABRB3 | PHF2 | LPCAT1 | MAP4K1 | MKLN1 | CDH9 | BIRC6 | OR10AD1 | WDR72 | SMG7 | CNFN | SRSF11 | CTSH | FREM3 | FOXN3 | SDHC | CCDC77 | PLXDC2 | GPC5 | SLC25A12 | EPC2 | CREB3L1 | MFN2 | LIN7B | ANKRD11 | AGAP2 | RIN3 | PIK3C2G | CYFIP1 | HERC2 | VIPR2 | SNX13 | KMT2D | HCN2 | SLC6A19 | HERC2P10 | KCNMB4 | GRID1 | PRKCB | HIVEP2 | BDNF-AS | TTC34 | AGAP1 | SCN1A | SCTR | CDH11 | KIAA0586 | CC2D2B | AFF2 | HMCN1 | STYK1 | ADGRE2 | PTPN11 | CREBBP | MEGF6 | FCGBP | CCDC157 | NRXN1 | MAP2K2 | EVC2 | FOXF2 | CRBN | RXRA | ADCY8 | IL4 | MLF1 | PDE2A | ATP2A2 | PLEKHG5 | BICD1 | SUV39H2 | LHX6 | MALRD1 | SKP2 | SPATA5L1 | TRIM27 | LMTK2 | TUBA8 | SAMD12-AS1 | HLA-DQB1 | RPS24 | TFB2M | G1786 | PPP5C | FGF19 | HTR6 | CDH18 | OR2L13 | CES1P2 | YJU2 | HSPB1 | DLX1 | HK1 | RFX1 | SEMA4A | ATP2A3 | KDM2B | HUWE1 | GRID2 | 5-Hydroxytryptamine Receptor 2 (5-HT2) (nonspecified subtype) | ARHGAP10 | AUP1 | PLA2G4E | TMPRSS9 | WDR26 | TRIM44 | ANKS1B | SLA | HEPACAM | ZFX | AXIN2 | DLX3 | ZNF594 | DLX4 | CEP89 | SDK2 | TMLHE | CHAT | HTR2C | CACNA1A | PTDSS1 | ITPA | SYNE1 | CDK14 | TPPP | GABRA5 | ITGB3 | FBXW4 | GPR61 | PPP2R2C | CHD8 | ACMSD | RYR3 | MCM2 | TH | ODAD4 | CNTNAP2 | ANAPC1 | SYNGAP1 | FARP1 | PSG1 | KCNMA1 | ALOX5 | NUDT7 | GRM1 | NRXN2 | ZFAND5 | CACNG2 | MOGAT1 | SLC1A1 | XRCC4 | P2RX7 | GNA14 | HSF2BP | SNAP25 | DOCK3 | NT5E | FAM172A | AOPEP | LINC01243 | OPALIN | ERBIN | DRD3 | GPR55 | ZNF568 | SYN1 | PGAM1 | ZMIZ1-AS1 | WDR35 | RAP1A | FANCF | DLX5 | AIRE | LNP1 | SLC6A1 | CDCA7 | HYDIN | DYRK1B | LANCL2 | SLC6A3 | FGF12 | G5728 | CNTN4 | XG | HELZ | NFAT5 | CHL1 | AS3MT | OXTR | BRIP1 | HTT | UBLCP1 | H1-4 | SETD1A | 5-Hydroxytryptamine Receptor (nonspecified subtype) | MAOB | KIFC1 | OR7A10 | POTEG | ATXN1 | SPDYC | PDE7B | SIN3A | ADAMTS18 | GABRA2 | MYO1A | SLC2A9 | HLA-DRB1 | ITPK1 | SNX29 | PTCHD1 | FAM91A1 | VRK2 | DEFB124 | MGAM | PIBF1 | GJD2 | TMIGD3 | OR10A2 | SLC25A48 | GAD1 | ABCB11 | PARPBP | GRIN2B | DDX3X | STAM | USP9X | KLHL7 | ADAMTS2 | NFKB1 | OPRM1 | GRM4 | ANK3 | TFB1M | GK5 | LINC00907 | LY86-AS1 | ANK2 | LRRC4C | ADRA1B | DSCAM | FAM227B | WDFY3 | ATP11B | PLEKHG1 | NID2 | PARK7 | PHF3 | LDB2 | BTBD9 | ANTXR2 | PRKN | PDE4D | ANKRD26P3 | ADCY1 | COL6A3 | LINC01060 | DPYD | ELP4 | WASF3 | OR5A2 | ABCC3 | MYO3A | PRKCE | ENOX2 | PTPRC | WNT1 | G2475 | SORL1 | ITPKB | DMD | IDE | OR52A5 | AP2B1 | LGALS1 | THRA | ACSBG1 | MAML3 | PRKG1 | PITX1-AS1 | PPP1R1A | RAB39B | OR51B6 | MYO5A | PPM1A | BDNF | TAAR1 | CDH23 | MIR29B2 | PLCH1 | PDE1A | ALOX15 | HOTAIR | CADPS2 | CSMD2 | Phosphodiesterase (nonspecified subtype) | C6orf141 | GPHN | HLA-B | RAP1B | ALDH1A3 | ZNF232 | KMT5B | ANKRD13C | RELN | MED12 | TXNDC16 | SV2B | ADCY9 | KCNQ2 | GALNT9 | IL1RAPL2 | DPYSL4 | MTUS2 | PDE3A | KIF26A | INTS6 | DNAJC28 | TAF1C | HTR1D | TAP2 | MIR4443 | HRH3 | Ribosomal Protein S6 Kinase, 70kDa (p70S6K) (nonspecified subtype) | KDM5A | SCN2A | KDM6A | CNOT3 | PITX1 | HTR7 | ZMIZ1 | CTNND2 | KLHDC10 | CAV3 | PPARG | COL14A1 | E2F8 | BBS1 | SH2D1A | PPARA | AMY2B | CD5 | TBC1D23 | BRD9 | DRD2 | MIR4761 | PPIA | AVPR1A | MICAL1 | TSC1 | ATP1A2 | NLGN1 | GABRA3 | CASC15 | G1956 | MTHFR | FOXN1 | ABCA12 | ECM2 | PRPF3 | DOCK10 | WDR46 | IQSEC2 | UBN2 | CYP4B1 | CDH4 | ADAR | CETP | RAP1GDS1 | SLC12A1 | OTX1 | IRF9 | GABRG1 | RAB11FIP5 | JMY | OR5L1 | HECTD4 | CACNA1H | DELEC1 | DNAH9 | EPHB1 | AIPL1 | PDE4B | RPTOR | NEBL | TRPM8 | KAT2B | ANKRD26P1 | CTBP2 | AK5 | PLCG2 | NRXN3 | G5562 | RASAL2 | ARHGAP32 | SOX2-OT | ASMT | CACNA1B | AHI1 | MFN1 | USP43 | PPP5D1P | ASXL1 | PLCB2 | TUBB3 | PACSIN1 | NCOR1 | COMT | ATP2B2 | CDK19 | ANP32A | ARHGEF16 | SGPL1 | NKAIN2 | PDLIM5 | KMT2C | MACROD2 | PHACTR1 | NEK3 | SPEN | PIK3CD | GPATCH1 | MBD5 | DNMT3A | TRPV1 | PER2 | OR51L1 | ZNF713 | PDZD2 | ST8SIA2 | ASAH2 | LLGL2 | TMEM192 | CACNA2D1 | TCF7L1 | OR2F1 | RYR1 | ADRA1A | MAP3K4 | ADCY10 | XIRP2 | MAOA | PTGFRN | G5743 | PTPRR | CNTN5 | PRKG2 | SLC12A2 | LINC01134 | KSR2 | CDH26 | ITPR2 | MED13L | OR51E2 | ANKRD31 | PLCB4 | GRM5 | SORBS1 | PLD5 | MAP2K1 | ARID1B | Serine/threonine-protein kinase (PAK) (nonspecified subtype) | CHST15 | AGT | TOP2B | MAD1L1 | CYP2D6 | AACS | DIAPH2 | FMR1 | GABBR1

疾病靶点研报
Autism Spectrum Disorders

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

Other Diseases

Apert Syndrome | Progressive Familial Intrahepatic Cholestasis | Goiter | Nail Disorder, Nonsyndromic Congenital | Reticular Dysgenesis | Martsolf Syndrome | Growth Hormone Excess | Hemochromatosis Type 1 | Primary Ovarian Insufficiency | Neuropathy | Oligoasthenoteratozoospermia | DICER1 Syndrome | Alopecia | Autosomal Recessive Congenital Ichthyosis | Delayed Sleep Phase Syndrome | McCune-Albright Syndrome | Antiphospholipid Syndrome | Cerebral Cavernous Malformations | Pouchitis | Myoclonus | Leukoplakia | Cholesteryl Ester Storage Disease | Ectopia Lentis, Isolated, Autosomal Recessive | Facioscapulohumeral Muscular Dystrophy | Adenosine Deaminase 2 Deficiency | Noonan Syndrome | Parkinson's Disease | Lymphoma Lymphoblastic | Hypermethioninemia | Vertebrobasilar Insufficiency | Methemoglobinemia Type IV | Esophageal Adenocarcinoma | Creatine Deficiency Syndrome Due To AGAT Deficiency | Tay-Sachs Disease | Scapuloperoneal Spinal Muscular Atrophy | Paternal Uniparental Disomy Of Chromosome 14 | Oligoastrocytoma | Spina Bifida | Oral Lichen Planus | Peutz-Jeghers Syndrome | Neonatal Progeroid Syndrome | Preaxial Polydactyly | Stuve-Wiedemann Syndrome | Smith-Magenis Syndrome | Myofibrillar Myopathy | Familial Hypobetalipoproteinemia | Mountain Sickness | Neurofibromatosis | Hyperkalemic Periodic Paralysis | Chondrodysplasia Punctata | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Shprintzen-Goldberg Syndrome | Agoraphobia | Crimean-Congo Hemorrhagic Fever | Arterial Tortuosity Syndrome | GLUT1 Deficiency Syndrome | Kohlschutter-Tonz Syndrome | Sclerosteosis 2 | POEMS Syndrome | Pontocerebellar Hypoplasia Type 2 | Globozoospermia | Combined Malonic And Methylmalonic Acidemia | CDKL5 Deficiency Disorder | Connective Tissue Disorders | Dental Caries | Colorectal Adenoma | Graves Disease | Lymphangiomatosis | Stroke, Ischemic | Carcinoma In Situ | Hypercholesterolemia | Myelofibrosis | Mucolipidosis | Tricho-hepato-enteric Syndrome | REM Sleep Behavior Disorder | Nephrosclerosis | NGLY1 Deficiency | Coloboma | Chondromyxoid Fibroma | Charcot-Marie-Tooth Disease Type 3 | Acromesomelic Dysplasia | Thrombocythemia, Essential | Essential Fructosuria | Waardenburg Syndrome Type 2A | Crohn's Disease | Graft-versus-host Disease | Metachromatic Leukodystrophy | HUPRA Syndrome | Macrophage Activation Syndrome | Generalized Epilepsy And Paroxysmal Dyskinesia | Constipation | Melanoma, Uveal | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Progressive Encephalopathy-optic Atrophy Syndrome | Nephrocalcinosis | Crisponi Syndrome | Charcot-Marie-Tooth Disease Type 4E | Nestor-Guillermo Progeria Syndrome | Hereditary Hemorrhagic Telangiectasia | Diabetes Mellitus, Transient Neonatal | Blastomycosis | Hypocalcemia | Glycogen Storage Disease Type 1a | Dupuytren Disease | Familial Digital Arthropathy-brachydactyly | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Blastoma, Pleuropulmonary | Myelomeningocele | Congenital Hereditary Endothelial Dystrophy Type II | Angioedema, Acquired | Ghosal Syndrome | Kidney Stones | Myositis, Focal | Harlequin Ichthyosis | Rett Syndrome | Perry Syndrome | Sarcoidosis | Cutis Laxa | Congenital Poikiloderma | Sepiapterin Reductase Deficiency | Urea Cycle Disorder | Avellino Corneal Dystrophy | Craniosynostosis | Benign Familial Pemphigus | Epidermolytic Ichthyosis, Annular | Chronic Granulomatous Disease, X-linked | Schwannomatosis | Infantile Neuroaxonal Dystrophy | Incontinentia Pigmenti | Neuroma | Central Core Disease | Colitis | Canavan Disease | Delirium | Anxiety Disorders | Gyrate Atrophy Of The Choroid And Retina | Atopy | Paronychia | Hereditary Pyropoikilocytosis | Tyrosine Hydroxylase Deficiency | Spinocerebellar Ataxia Type 3 | Focal Cortical Dysplasia Type 2 | Bicuspid Aortic Valve | Ocular Albinism Type 1 | Supravalvular Aortic Stenosis | Bulimia Nervosa | Spinocerebellar Ataxia Type 7 | Trichothiodystrophy | Primary Erythromelalgia | Congenital Stromal Corneal Dystrophy | COACH Syndrome | Tatton-Brown-Rahman Syndrome | Charcot-Marie-Tooth Disease Type 2D | Limb Girdle Muscular Dystrophy | Fukuyama Congenital Muscular Dystrophy | Uremia | Jacobsen Syndrome | Niemann-Pick Disease, Type B | Allan-Herndon-Dudley Syndrome | Keratosis | Melnick-Needles Syndrome | Congenital Aniridia | Dominant Optic Atrophy | Takenouchi-Kosaki Syndrome | Primary Hyperoxaluria Type 1 | CHARGE Syndrome | Melanoma | Intellectual Disability, Autosomal Dominant 5 | Vertigo | Inflammatory Linear Verrucous Epidermal Nevus | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Nephropathy | Esophagitis | Amelanotic Melanoma | Chronic Granulomatous Disease | Hemophagocytic Lymphohistiocytosis | WAGR Syndrome | Osteogenesis Imperfecta Type I | Sick Sinus Syndrome 1 | Glycogen Storage Disease | Endometritis | Spondyloperipheral Dysplasia | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Desbuquois Syndrome | Enlarged Vestibular Aqueduct | Twin-to-twin Transfusion Syndrome | DNA Ligase IV Deficiency | Maple Syrup Urine Disease | Reflex Epilepsy | Lung Diseases | Hepatoblastoma | Vasculitis | Alopecia Areata | Keloid | ICF Syndrome | Charcot-Marie-Tooth Disease Type 4D | Familial Advanced Sleep Phase Syndrome | Meningioma, Benign | Wolfram Syndrome | Anal Fissure | Cancer, Prostate | Malnutrition | Autism Spectrum Disorders | Hypotrichosis | Pseudohypoparathyroidism Type 1B | Anorectal Malformations | Chronic Myeloid Leukemia | Gestational Trophoblastic Disease | Aarskog-Scott Syndrome | Diabetes Insipidus | Chronic Leukemia | Meningococcal Meningitis | Autosomal Recessive Spastic Paraplegia Type 54 | Congenital Stationary Night Blindness | Robinow Syndrome | Sjogren Syndrome | Gardner Syndrome | Multiple Sulfatase Deficiency | Trimethylaminuria | Cholangiocarcinoma | Nephritis, Interstitial | Hepatitis A | Leukemia | Neurodevelopmental Disorders | Exfoliative Dermatitis | Renal-hepatic-pancreatic Dysplasia | CEDNIK Syndrome | Marinesco-Sjogren Syndrome | Glutaric Aciduria Type 3 | Congenital Diaphragmatic Hernia | Wieacker-Wolff Syndrome | Acute Tubular Necrosis | Ataxia-ocular Apraxia 2 | Splenomegaly | Carcinoma, Small Cell | Allergic Contact Dermatitis | Leukodystrophies | Seasonal Mood Disorder | Nanophthalmos | Hepatitis, Chronic | Corneal Dystrophies, Hereditary | Light Chain Amyloidosis | Arthritis, Psoriatic | Acquired Partial Lipodystrophy | Leukocyte Adhesion Deficiency | Usher Syndrome Type II | Sertoli Cell-only Syndrome | Vitelliform Macular Dystrophy | Dengue Shock Syndrome | Optic Nerve Hypoplasia, Bilateral | Meningococcal Infections | Intermittent Explosive Disorder | Familial Partial Lipodystrophy | Juvenile Hyaline Fibromatosis | Dengue Hemorrhagic Fever | Dysplastic Nevus | Pompe Disease | Hypopituitarism | Erectile Dysfunction | Cardiospondylocarpofacial Syndrome | Lyme Disease | Hepatitis B, Chronic | Compartment Syndrome | Aspartylglycosaminuria | Polycystic Liver | Riboflavin Transporter Deficiency Neuronopathy | Cone Dystrophy | PASLI Disease | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Retinopathy, Diabetic | Diabetes Gestational | Anovulation | Isovaleric Acidemia | Methemoglobinemia | Chronic Lymphocytic Leukemia | Non-Langerhans Cell Histiocytosis | Bladder Exstrophy | Lymphoproliferative Disorders | McKusick Type Metaphyseal Chondrodysplasia | Benign Recurrent Intrahepatic Cholestasis 1 | Hypersomnia | Schizoaffective Disorder | Larsen Syndrome | Prolidase Deficiency | Congenital Mirror Movements | Acute Motor Axonal Neuropathy | Urethritis | Sarcoma, Ewing | Diabetic Nephropathy | Spinocerebellar Ataxia Type 31 | Intracerebral Hemorrhage | Hypogammaglobulinemia | Multicystic Renal Dysplasia | Scleroderma | Duane Retraction Syndrome | Herpes Genitalis | Diabetic Neuropathy | Pseudohypoaldosteronism | Congenital Central Hypoventilation Syndrome | Agranulocytosis | Sweet Syndrome | Smoldering Myeloma | Cervicitis | Pleurisy | Peripheral Neuropathy | Blepharoconjunctivitis | Primary Progressive Nonfluent Aphasia | Epidermolytic Hyperkeratosis | Alagille Syndrome | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Carbamoyl Phosphate Synthetase I Deficiency | Adenomatoid Tumor | Pneumococcal Meningitis | Ocular Hypertension | Priapism | Encephalopathy | Prolactinoma | Carey-Fineman-Ziter Syndrome | Exostoses | Chylomicron Retention Disease | Hamartoma | Anterior Segment Dysgenesis | Hartnup Disease | Hyper IgE Syndrome | Acrodermatitis Enteropathica | Obesity, Morbid | Retinal Dystrophy | Pigment Dispersion Syndrome | Intermittent Claudication | Pulmonary Vein Stenosis | Pathological Gambling | Hodgkin Lymphoma | Distal Myopathy | Haim-Munk Syndrome | Mitochondrial Myopathy | Stroke | Muir-Torre Syndrome | Multiple Myeloma | Osteopetrosis | Tracheal Disorders | Nicotine Dependence | Paracoccidioidomycosis | Isobutyryl-CoA Dehydrogenase Deficiency | Myelodysplasia | Nasodigitoacoustic Syndrome | Congenital Nephrotic Syndrome | Peritonitis | Jaundice, Obstructive | Systemic Mastocytosis | Diarrhea | Thrombosis | Autonomic Nervous System Disorders | Cohen Syndrome | Alveolar Capillary Dysplasia | Atopic Dermatitis | Plasma Cell Dyscrasia | Ureteropelvic Junction Obstruction | Blepharospasm | Progressive Familial Intrahepatic Cholestasis Type 1 | Nephrotic Syndrome | Lennox-Gastaut Syndrome | Parapsoriasis | Fibrodysplasia Ossificans Progressiva | Sleep Disorder | Hereditary Folate Malabsorption | Beckwith-Wiedemann Syndrome | Lattice Corneal Dystrophy Type 1 | Hypersensitivity Pneumonitis | Optic Neuropathy | Hereditary Hemorrhagic Telangiectasia Type 2 | Antisynthetase Syndrome | Venous Insufficiency | X-linked Creatine Transporter Deficiency | Barakat Syndrome | Retinal Detachment | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Nemaline Myopathy 8 | Atrial Septal Defect | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Ileitis | Adams-Oliver Syndrome | Gastritis | Uveitis | Mandibuloacral Dysplasia With Type A Lipodystrophy | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Cyclic Vomiting Syndrome | Rosacea | Atrioventricular Septal Defect | Greig Cephalopolysyndactyly Syndrome | Myoclonic Atonic Epilepsy | Tendinitis | Acute Anterior Uveitis | Spinocerebellar Ataxia Type 40 | Intestinal Hypomagnesemia 1 | Pineoblastoma | Mannosidase Deficiency Diseases | Sarcoma | Lipoma | Multiple Sclerosis, Relapsing-remitting | Ollier Disease