Glioblastoma

About the Disease
Glioblastoma, also known as glioblastoma multiforme, is related to brain cancer and glioma, and has symptoms including headache and seizures. An important gene associated with Glioblastoma is MIR21 (MicroRNA 21), and among its related pathways/superpathways is miRNAs involved in DNA damage response. The drugs Trametinib and Dabrafenib have been mentioned in the context of this disorder. Affiliated tissues include brain, t cells and eye, and related phenotypes are glioblastoma multiforme and abnormal cell morphology

Common Targets
MEDAG | APC | ISL1 | CBLN1 | HLA-DQB1 | CTNNB1 | ADAM32 | GDNF | MYNN | PSMA2 | IDUA | RAB6C | DNA-Directed DNA Polymerase Complex | CLEC2L | MCAM | G472 | PNMT | POLD1 | CYBA | MIR20A | OR5AR1 | ABL1 | HEATR3 | Vascular endothelial growth factors (VEGF) (nonspecified subtype) | TERF2 | G1956 | G0S2 | H3-3A | JAK2 | NBN | ZMYND10 | DCLRE1B | G3845 | MLH1 | SHANK1 | PDHX | RNF135 | RECQL4 | LMF1 | EDNRA | STN1 | MDM4 | PARP3 | CCDC26 | LDLR | ZBTB16 | ALPL | CORO6 | CNGA3 | STEAP4 | THAP4 | ADGRL4 | H3-3B | SDC1 | EXO5 | CD24 | TCEA3 | B3GNT7 | HOXD8 | FOLR2 | SOCS1 | GNAL | ATG2B | MARVELD2 | FAP | NPTX2 | LIMD1 | PRR15 | PRRT1 | G6774 | CD27 | ONECUT2 | G7015 | NOTCH3 | MEGF10 | AHDC1 | DDX23 | TTC12 | MAP2 | CSK | SRRM3 | TOM1L1 | TFRC | LCLAT1 | KIAA1614 | TBX1 | TUBA4B | MEG3 | G4089 | BTK | HDAC6 | ERCC1 | VAV1 | ARCN1 | SSTR2 | MAP4 | IL13RA2 | SMO | CNTN2 | ME1 | ITGA10 | RYR1 | DGAT1 | GRIN1 | Integrin alphavbeta3 (vitronectin) receptor | LUM | FGFR2 | GHSR | PCDH11X | CYSLTR1 | SFRP2 | CBLN3 | Phosphodiesterase IV (PDE4) (nonspecified subtype) | TBR1 | BNC1 | CYTOR | LGALS3 | THRB | VILL | SOST | CCND2 | GSTM5 | NXPH4 | BMP4 | PLA2G4A | OR5P2 | G595 | LRFN5 | SLC16A8 | HIF1A | ADRA1A | NR1H2 | PARP9 | PAMR1 | KMT2C | FAT1 | RAD52 | NLRP5 | RPS6KA3 | DRD4 | SEMA3E | HNRNPA2B1 | KEL | LZTR1 | CDK6 | MYL12A | BCAN | NRAS | SCGB3A1 | HRAS | MIR10B | MIR137 | SLC7A5 | OBSCN | ATRX | GRIA1 | AKAP6 | NEUROD1 | C1QTNF12 | KLHL35 | Protein Kinase B (PKB/Akt) (nonspecified subtype) | CNR2 | NF-kappaB (NFkB) | TGFB1 | VEGFC | XRCC2 | TMED7-TICAM2 | AXL | LY6H | LRRC55 | HNRNPF | CLSTN1 | CA1 | FAM229A | HER (erbB) (nonspecified subtype) | G207 | SLC35G2 | MAPK6P2 | TNC | NRG2 | AGT | TAFA1 | GFI1 | HOXD13 | SCD | CD3 Complex (T Cell Receptor Complex) | SLC26A3 | G7099 | G5133 | GRM6 | ISM1 | CSF1R | APLNR | ACSL1 | RAPGEFL1 | NR1H3 | AREG | POLE | KIT | DLGAP3 | G1950 | AP4B1 | ZNF99 | Lipoxygenase (nonspecified subtype) | CDK4 | RBBP4 | ATG5 | RCOR1 | FPR1 | TNFRSF18 | CDKN2B | G29126 | TUBA3D | RAD54B | GLI3 | G5728 | MOG | CYTB | TBX18 | IL4R | KCNS2 | MAOA | TOP1 | IDH1 | G4780 | UNC13A | IPO4 | FZD6 | TUBA3C | G7852 | PMS2 | SPTA1 | TJP1 | GRIA2 | TACC3 | HLA-B | ARID2 | TP73 | ATP5MC2 | DDR2 | MIR375 | CELF5 | MRC1 | G4851 | PDE10A | BCR | BRCA2 | CELF4 | TRPM8 | PIK3R1 | ATG16L1 | NR4A1 | CYP11A1 | HOXA11 | NOD2 | UGT2B4 | IER3 | HLA-DRB1 | LOC145845 | NOTCH4 | HPDL | SPACA6 | EMP3 | HLA-J | MT1M | PHLDB1 | PIK3C2A | CACNG8 | SERPINB1 | CD200 | FGFR3 | COL9A2 | EPHB4 | IQSEC1 | FLOT1 | NKD1 | CNR1 | WIF1 | G673 | HLA-L | SFRP4 | DKK1 | CACNA1C | LYL1 | NFKBIA | ROS1 | LINC02610 | TMEM26 | RTL4 | MAL | EYA4 | CDKN2B-AS1 | PDPN | NDRG2 | CLIC1 | Integrin alpha5beta1 (VLA-5) receptor | PMEL | FABP3 | WDR7 | ROBO4 | DHRSX | CA7 | G4137 | MIR328 | TRPV2 | IL15 | Estrogen receptor (nonspecified subtype) | PXDN | G1029 | ENO1 | NPM2 | PDGFRB | TOX2 | ANGPT2 | ID4 | Integrin alphavbeta5 receptor | EDNRB | TPBG | G142 | PIK3C2B | Histone acetyltransferase (HAT) (nonspecified subtype) | NSD1 | KLRK1 | LAMP1 | MIR21 | WNK2 | INA | ACRBP | DNAH1 | TFAP2A | LRRC31 | SEPTIN9 | TET2 | APBA2 | Tyrosine Kinase (nonspecified subtype) | Reverse transcriptase (Telomerase) | LRRC3B | EPHA3 | RNPC3 | PIKFYVE | CMYA5 | TRPV1 | G4609 | C1orf94 | DPP10 | EFEMP1 | TET1 | RPP25 | ZBED3 | PPARG | ANO2 | PTGS1 | COL1A2 | STK11 | POT1 | TREM2 | TP73-AS1 | LHX5 | SOCS3 | HLA-A | ACTR3C | DCT | RNF39 | PIK3C2G | PTPN1 | SKOR1 | ZNF655 | RHBDF2 | PYCARD | JAG1 | AKT2 | F2 | PRR16 | QPCT | NTRK1 | LOC100287944 | GSK3B | TSPO | AXIN1 | KIF5C | NRP1 | DCX (DDB1-CUL4-X-box) E3 protein ligase complex | G2475 | GSDMB | KCNIP3 | MTSS1 | KHDRBS2 | ATG4B | CD70 | IL5 | SMARCA4 | DDIT3 | M1AP | SEMA3C | PSMD10 | ARL9 | XRCC3 | ITGA7 | RTEL1 | TES | B3GALT4 | RASGRP2 | MACROD1 | GSTT1 | ACKR3 | AOX1 | LAD1 | ENO2 | NFIL3 | CDH18 | PCDHGA4 | FLT4 | MAML2 | G3480 | RBP1 | NRXN1 | ALS2CL | mTOR complex 2 | HUWE1 | SPEG | PDE4C | POLR3B | NUAK1 | NEFM | G6PC1 | CPQ | NTN1 | BCAT1 | MOXD1 | KIF11 | IL18RAP | IDH2 | Vascular endothelial growth factor receptor (VEGFR) (nonspecified subtype) | PIK3C3 | CCDC68 | PDLIM4 | COPS5 | HPS1 | Platelet-Derived Growth Factor Receptor (nonspecified subtype) | KDM1A | FLT1 | ADAM12 | RAVER2 | CLCN3 | LINC00092 | RAD51 | NR2F2 | MCF2L2 | WFDC2 | G7157 | FMOD | NFKBIZ | CD3E | SEMG1 | FGFR1 | KLRC4-KLRK1 | SST | FBP1 | HSD11B2 | MARS1 | PKM | SFRP5 | RASSF10 | LINC01341 | ACTG1 | PROM1 | MSC | HEY1 | AOPEP | SLC4A4 | GJB6 | CHI3L1 | LIF | TGFB2 | DNA topoisomerase (nonspecified subtype) | DGKA | TEK | EPHA2 | AP-1 Transcription Factor Complex | LRRC15 | FGFR4 | DDN | TMEM235 | APEX1 | GJA1 | CLCN5 | Poly [ADP-ribose] polymerase (nonspecified subtype) | TXNRD1 | PRKCB | PVR | RB1 | IRF6 | G4193 | TMEM97 | SCD5 | MYO15B | RBP7 | Integrin alpha7beta1 Receptor | MBP | PLA2R1 | PACS2 | PAX6 | IL12A | DSC3 | Inosine 5'-monophosphate dehydrogenase (IMPDH) (nonspecified subtype) | PTH1R | Tubulin | RFX4 | FASLG | CPNE8 | LZTS2 | NIPAL4 | CBLN4 | EPHA5 | TNXB | TPPP3 | EPHA10 | SCN9A | SHH | TAMALIN | TNFRSF4 | CCSER1 | VRK2 | ULK2 | HOXC4 | ZAR1 | PDE4A | SEL1L | GSX2 | MMP8 | TAPBPL | TIGIT | PGF | Integrin alpha-10/beta1 | PIDD1 | ACTA1 | DHX33 | G1786 | ERBB4 | PDHA1 | SEMA3A | HLA-DPB1 | CPEB1 | GRAMD2A | FANCA | CTLA4 | G5743 | NF1 | G3082 | ZNF704 | SELENOP | Integrin alphavbeta1 | GRID2IP | G4233 | WT1 | PIK3CA | CCNI2 | UGT2A3 | CRACR2A | PARP2 | RRAS | PPP1R14A | SLC34A2 | HPSE2 | NT5E | CPLX1 | G7124 | NSUN7 | ATG10 | VAX2 | CRACDL | NID2 | CLHC1 | SMARCB1 | HCAR2 | SFRP1 | IL-13 receptor | ETFA | G367 | G2064 | MUS81 | G672 | EPHX3 | CALCR | FLT3 | ULBP1 | CFTR | ALB | DRC1 | SSTR1 | NBL1 | FYN | SEC31B | RHOD | MYCN | TRPA1 | HTR2A | BST2 | MIF | AKT3 | GNMT | LPCAT2 | BIRC5 | FTO | COL21A1 | HPGDS | GRPR | PPP1R36 | SLC2A3 | PDGFRA | FCHSD1 | DCLRE1A | PTPN11 | GABRA6 | RGMA | C2orf80 | TRAF3IP2 | SERPING1 | IL10 | GSTM1 | OPCML | RET | CX3CR1 | OR5D13 | H3C2 | DKK3 | TOP2A | VHL | CFLAR | MGMT | G5243 | MIR196A2 | G2146 | ALDH1A3 | VTI1A | RHBDF1 | GOLGA3 | AKR7A3 | ALOX5 | IL4 | KIR2DS4 | PLAUR | DLL4 | MICA | PSD | RTEL1-TNFRSF6B | RPL5 | CRIP1 | SNX31 | CD276 | ONECUT1 | COL11A2 | MYADM | ULK1 | SIX3 | CYP19A1 | SCARNA5 | OR5D18 | ADGRA2 | EPAS1 | PPM1D | HOTAIR | G238 | HOXA5 | RAB27B | IL13 | KCNB1 | NEIL3 | G7422 | LRIG1 | CER1 | ANXA2 | EVX2 | RAD54L | SOX2-OT | DKK2 | GSTP1 | STAG2 | HLA-C | ZMIZ1 | Fibroblast Growth Factor Receptor (FGFR) (nonspecified subtype) | MIR199A1 | MYRIP | G5347 | GPR55 | MAGI2 | RAD51B | CMTM2 | GAREM2 | MSH6 | HMOX1 | FAM83F | IDO2 | MIR199A2 | CRBN | SSH3 | PICK1 | MSH2 | OR8K3 | KDR | PIK3CG | H2AC25 | NKAIN2 | TCF7L2 | XRCC1 | YES1

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

Other Diseases

Ectopia Lentis, Isolated, Autosomal Recessive | Antenatal Bartter Syndrome Type 1 | Withdrawal Syndrome | Oguchi Disease-2 | Basal Cell Nevus Syndrome | Premature Ejaculation | Spinocerebellar Ataxia Type 10 | Subacute Sclerosing Panencephalitis | Anovulation | Aplastic Anemia | Primary Pigmented Nodular Adrenocortical Disease | Angioimmunoblastic T-cell Lymphoma | Cranial Nerve Disease | Diabetes Type 2 | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Alopecia Areata | High Molecular Weight Kininogen Deficiency | Molybdenum Cofactor Deficiency | Carey-Fineman-Ziter Syndrome | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Paracoccidioidomycosis | Sick Sinus Syndrome 1 | Fukuyama Congenital Muscular Dystrophy | Acne | Carney Triad | Poretti-Boltshauser Syndrome | Optic Neuropathy, Anterior Ischemic | HIBCH Deficiency | Spinocerebellar Ataxia Type 8 | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Nephritis, Interstitial | Kohlschutter-Tonz Syndrome | Immunoproliferative Disorders | Cataplexy | Noonan Syndrome-like Disorder With Loose Anagen Hair | Thrombocythemia, Essential | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Pituitary Dwarfism | Niemann-Pick Disease, Type A | Gyrate Atrophy Of The Choroid And Retina | Marshall-Smith Syndrome | Bardet-Biedl Syndrome | Sensorineural Hearing Loss | Herpes Simplex Dermatitis | Low Phospholipid Associated Cholelithiasis | Glutaric Aciduria Type 1 | Adrenomyeloneuropathy | Neurotoxicity | Hartnup Disease | Galloway-Mowat Syndrome | Familial Retinal Arterial Macroaneurysm | Fibromyalgia | Eosinophilia | Spinocerebellar Ataxia Type 7 | Lennox-Gastaut Syndrome | Pseudohypoparathyroidism Type 1C | Lichen Sclerosus | Congenital Dyserythropoietic Anemia Type 4 | Kabuki Syndrome 2 | Chondroma | Craniometaphyseal Dysplasia | Pemphigus Vulgaris | Colorectal Adenoma | Hyperuricemic Nephropathy, Familial Juvenile | Aromatic L-amino Acid Decarboxylase Deficiency | Schnyder Crystalline Corneal Dystrophy | Cerebellar Ataxia, Cayman Type | Mabry Syndrome | Presbyopia | Primary Carnitine Deficiency | Leiomyoma | Sleep Apnea, Obstructive | Wolcott-Rallison Syndrome | Primary Hyperoxaluria Type 1 | Pendred Syndrome | Fibrosis | Anorexia Nervosa | Arthropathy | Acanthosis Nigricans | Leri-Weill Dyschondrosteosis | Inflammatory Joint Disease | Beckwith-Wiedemann Syndrome | Retinitis | Polycythemia | Crisponi Syndrome | Silicosis | Retinal Telangiectasia | Malaria | Polyomavirus Nephropathy | Hemangioblastoma | Blomstrand Osteochondrodysplasia | Hepatitis E | Blepharospasm | Rickets | Muscle Wasting | Alstrom Syndrome | Lymphoma Lymphoblastic | Carbohydrate Metabolism Disorders | Lymphangioma | Kabuki Syndrome | Chronic Periodontitis | Pulmonary Stenosis | Schizophrenia | Rothmund-Thomson Syndrome | Vertebrobasilar Insufficiency | Hypopigmentation | Conduct Disorder | Malignant Fibrous Histiocytoma | Sarcoidosis | Hydronephrosis | Pemphigus Foliaceus | Lathosterolosis | Osteogenesis Imperfecta Type V | Dermatitis | Gallstones | Acne Vulgaris | Pre-eclampsia | Meningeal Melanocytoma | Hyperlipidemia | Cardiomyopathy, Hypertrophic | Farber Disease | Benign Familial Neonatal Convulsions | Pneumococcal Meningitis | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Orthostatic Intolerance | Pseudomyxoma Peritonei | Guillain-Barre Syndrome | Urticaria | C3 Glomerulonephritis | Oligoasthenoteratozoospermia | Vitreoretinal Degeneration, Snowflake Type | Alpha-1 Antitrypsin Deficiency | Gout | Neuronal Ceroid Lipofuscinosis | Fibrosarcoma | Toxoplasmosis | Transcobalamin Deficiency | Mucolipidosis | Sarcomatoid Carcinoma Of The Lung | Ichthyosis Bullosa Of Siemens | Wolfram Syndrome 2 | Oculocutaneous Albinism Type 1 | Optic Nerve Diseases | Myasthenia | Spinocerebellar Ataxia Type 40 | Crimean-Congo Hemorrhagic Fever | Anal Fissure | Cerebral Amyloid Angiopathy | Progressive Familial Intrahepatic Cholestasis Type 3 | Basal Ganglia Cerebrovascular Disease | Chorea | Congenital Heart Defects | Smith-Magenis Syndrome | Priapism | Pyruvate Decarboxylase Deficiency | Hypertension, Portal | Bacterial Meningitis | Retinal Diseases | Chromosome 16p11.2 Deletion Syndrome | Chiari Malformation Type I | Prader-Willi Syndrome | Spondylocarpotarsal Synostosis Syndrome | Pneumonia, Bacterial | Chudley-McCullough Syndrome | Schaaf-Yang Syndrome | Glycogen Storage Disease Type 0, Muscle | Pseudohypoaldosteronism | Hypersensitivity Pneumonitis | Sulfite Oxidase Deficiency | Bronchitis, Chronic | Schwannoma | Hepatitis, Alcoholic | Sarcoma | Succinic Semialdehyde Dehydrogenase Deficiency | Trimethylaminuria | Axenfeld-Rieger Syndrome | SAPHO Syndrome | Duane Retraction Syndrome | Postaxial Polydactyly | Congenital Stationary Night Blindness | Focal Dermal Hypoplasia | X-linked Creatine Transporter Deficiency | Adrenal Insufficiency | Uremia | Neurodegeneration With Brain Iron Accumulation | Stroke | Brachydactyly | Zygomycosis | Zimmermann-Laband Syndrome | Hyperphenylalaninemia | Chronic Mucocutaneous Candidiasis | Gaucher Disease | Dystrophy, Cone-rod | Renal Tubular Dysgenesis | Chromosome 17q21.31 Deletion Syndrome | CDKL5 Deficiency Disorder | Fascioliasis | Cystinosis | Scapuloperoneal Spinal Muscular Atrophy | Lissencephaly 2 | Bladder Exstrophy | Schizencephaly | Prostatitis | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Orotic Aciduria | Maple Syrup Urine Disease | Kaposiform Hemangioendothelioma | Osteitis | Blue Nevus | Thanatophoric Dysplasia | Familial Pheochromocytoma-paraganglioma | Non-epidermolytic Palmoplantar Keratoderma | Purpura, Thrombotic Thrombocytopenic | Pulmonary Veno-occlusive Disease | Dermatofibrosarcoma | Adenosine Deaminase Deficiency | Methylmalonic Acidemia | Achromatopsia | Cannabis Abuse | Metaphyseal Chondrodysplasia, Schmid Type | Neuromyelitis Optica | Patent Foramen Ovale | Hereditary Inclusion Body Myopathy | Parkinsonism | Kernicterus | Cancer, Lung | Spina Bifida | Porencephaly | Potocki-Shaffer Syndrome | FG Syndrome | Hypopituitarism | Hemochromatosis Type 1 | Pearson Syndrome | Long QT Syndrome Type 3 | Citrullinemia | Psoriasis | Syncope | Adams-Oliver Syndrome | Intestinal Hypomagnesemia 1 | Waardenburg Syndrome Type 2 | Congenital Absence Of Vas Deferens | Neurofibromatosis Type 1 | Endophthalmitis | Hemolytic Anemia | Conjunctivitis | Arthrogryposis | Pneumonia, Viral | Warsaw Breakage Syndrome | Arthritis, Gouty | Trismus-pseudocamptodactyly Syndrome | H Syndrome | MELAS Syndrome | Cardiospondylocarpofacial Syndrome | Macular Corneal Dystrophy | Pancytopenia | Vitiligo | Lipoma | Micropenis | Methylmalonic Aciduria And Homocystinuria, CblC Type | Primary Erythromelalgia | Melanoma, Malignant | Colitis, Collagenous | Von Hippel-Lindau Disease | Hypoparathyroidism | Amyloidosis | Polyarteritis Nodosa | Syphilis | Renal Hypouricemia | Scleroderma, Diffuse | Craniosynostosis | Odonto-onycho-dermal Dysplasia | Riboflavin Transporter Deficiency Neuronopathy | Echinococcosis | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | IgA Nephropathy | Pelvic Inflammatory Disease | Retinal Coloboma | Rhabdomyosarcoma, Alveolar | Epiphyseal Chondrodysplasia, Miura Type | Absence Epilepsy | Dent Disease | Malignant Peripheral Nerve Sheath Tumor | Metatropic Dysplasia | Oculodentodigital Dysplasia | DEND Syndrome | Pontocerebellar Hypoplasia Type 2 | Frontometaphyseal Dysplasia | Chondromyxoid Fibroma | Goldenhar Syndrome | Leukoplakia | Dentinogenesis Imperfecta | Cerebrovascular Disorders | Pericarditis | Sturge-Weber Syndrome | Costello Syndrome | Hyperparathyroidism-jaw Tumor Syndrome | Cardiac Arrest | Rhabdomyosarcoma | Usher Syndrome Type I | Iron Deficiency Anemia | Renal Oncocytoma | Polycystic Kidney, Autosomal Recessive | Occipital Neuralgia | Familial Isolated Hyperparathyroidism | Wieacker-Wolff Syndrome | Larsen Syndrome | Acromicric Dysplasia | Nephrotic Syndrome | Meningioma, Benign | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Varices | Adrenoleukodystrophy, X-linked | Cutis Laxa | Li-Fraumeni Syndrome | Ghosal Syndrome | Congenital Hereditary Endothelial Dystrophy Type II | Lesch-Nyhan Syndrome | Spinocerebellar Ataxia Type 38 | Spinocerebellar Ataxia Type 15 | Early Infantile Epileptic Encephalopathy 28 | Pigment Dispersion Syndrome | Vitamin B12 Deficiency | Congenital Torticollis | Urolithiasis | Infantile Spasm | Familial Episodic Pain Syndrome | Pleurisy | Cabezas Syndrome | Pure Autonomic Failure | Hypercholesterolemia | Platelet Disorders | Autosomal Recessive Spastic Paraplegia Type 35 | Astrocytoma, Anaplastic | Waardenburg Syndrome | Peutz-Jeghers Syndrome | Abetalipoproteinemia | Intestinal Obstruction | Split Hand-foot Malformation | Sjogren Syndrome | Exfoliative Dermatitis | Impetigo | ICF Syndrome | Autosomal Recessive Spastic Paraplegia Type 54 | Granular Corneal Dystrophy Type 1 | Erythropoietic Protoporphyria | Pneumonia, Mycoplasma | Limb Girdle Muscular Dystrophy | Paronychia | Hypospadias | Pain | Congenital Adrenal Hyperplasia 1 | Cholangiocarcinoma | Veno-occlusive Disease | Antithrombin III Deficiency | Amelanotic Melanoma | Astrocytoma | Hernia, Inguinal | Pulverulent Zonular Cataract | Alzheimer Disease, Late Onset | Osteosclerosis | Sitosterolemia | Schizoaffective Disorder | Mitochondrial Myopathy | Seasonal Mood Disorder | Posterior Polar Cataract | Hydrocephalus | Spondylosis | Combined Deficiency Of Factor V And Factor VIII | Pituitary Disorders | Dysmorphophobia | Hereditary Mixed Polyposis Syndrome | Adenoma, Pituitary | Basal Ganglia Disease | Pulmonary Sclerosing Hemangioma | Pantothenate Kinase-associated Neurodegeneration | Congenital Disorders Of Glycosylation | Sclerosteosis | Silver-Russell Syndrome | Pyruvate Kinase Deficiency | Binge Eating Disorder | Holoprosencephaly | Episodic Ataxia | Lymphangioleiomyomatosis | Stroke, Ischemic | Leukocyte Adhesion Deficiency | Congenital Hereditary Endothelial Dystrophy Type I | Nanophthalmos | Congenital Hemolytic Anemia | Bone Giant Cell Tumor | Cystitis | Still Disease | Primary Sclerosing Cholangitis | Glomerulonephritis | Micro Syndrome | Scleroderma | Hyperthyroidism | Leukoencephalopathy, Progressive Multifocal | Methemoglobinemia | Craniofrontonasal Syndrome | Familial Exudative Vitreoretinopathy