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297 Genes or Implicated Loci to Visit
181 Syndromes or Related Conditions
ABCA1  ABCC8  ABCC9  ACE  ACTN4  ADA  ADPRT  ADRB2  ADRB3  AGER  AGPAT2  AGT  AIRE  AKR1B1  AKT2  ALDRL6  ALMS1  ALOX12  ANGPTL3  ANGPTL4  APCS  APM1  APOA1  APOC2  APOE  APP  AQP2  AQP3  AQP4  ARHGAP4  ART1  ASIP  AUTS1  AVP  AVPR1A  AVPR1B  BBS3  BBS4  BCHE  BF  BMIQ3  BMIQ4  BSCL2  BTK  C4A  CAPN10  CAQ14  CAQ5  CAT  CAV1  CAV2  CBLB  CCK  CCKAR  CCL21  CCR7  CD1D  CD36  CD3E  CD59  CD8A  CD  CDK4  CETP  CFLAR  CFTR  CHGA  CIDEA  CLCNKA  CNTF  COL1A1  CP  CPE  CPS1  CREB1  CTLA4  CX3CR1  CXCR3  CYP2C9  DGS  DLL1  DPP4  EEC1  EIF2AK3  ENPP1  ENSA  F2  FABP2  FABP4  FBP1  FOXC2  FOXO1A  FOXP3  FRDA2  FRDA  FUT7  GAD1  GAD2  GAD3  GANC  GC  GCCR  GCG  GCGR  GCK  GCKR  GDF8  GEM  GIP  GIPR  GJA4  GLA  GP1BA  GPD2  GPR1  GPR35  GSK3A  GSK3B  GYS1  GZMA  HBA1  HBB  HDLC2  HFE  HK2  HLA-DQA1  HLA-DQB1  HLA-DRA  HMGA2  HNF4A  HPE1  HS  HSD11B1  HSD17B7  HTR2C-PUTATIVE  HYMAI  IAPP  ICA1  IDDM10  IDDM11  IDDM12  IDDM13  IDDM15  IDDM17  IDDM18  IDDM3  IDDM4  IDDM5  IDDM6  IDDM7  IDDM8  IDDM  IDE  IGAD1  IGF1  IGF1R  IGRP  IKBKB  IL10  IL18  IL1A  IL1RN  INS  INSR  IPF1  IRDN  IRS1  IRS2  IRTF1  ISL1  ITGB3  JBS  JK  KCNE2  KCNJ11  KHK  KIRREL2  LAMP2  LDHB  LEP  LEPR  LIG4  LMNA  LPL  LRP5  LSL  MAPK8IP1  MAPK8IP2  MC2R  MC3R  MC4R  MGST3  MICA  MKKS  MLRG  MTTE  MTTH  MTTI  MTTK  MTTL1  MTTQ  MTTS2  MUT  NDP  NEUROD1  NEUROG3  NF1  NIDDM2  NKX2B  NOS2A  NPY  NR0B2  OCRL  OGT  OXCT  OXT  PAI1  PAOD1  PBX1  PCK1  PCSK1  PDE3B  PEA15  PECI  PFKFB3  PFKM   PGR  PLAGL1  PLIN  PON1  PON2  PPARA  PPARD  PPARG  PPARGC1  PPGB  PPP1R2  PPP1R3A  PROS1  PRPH  PRPS1  PRPS2  PRSS16  PSMB8  PTPN1  PTPRC  PTPRN2  PTPRN  PTTG1  RECQL2  REG1A  RETN  RNPEPL1  RPS6KA1  RRAD  SCYA2  SDAM  SEDL  SEL1L  SHC1  SIAT9  SLC19A2  SLC2A10  SLC2A1  SLC2A2  SLC2A4  SLC38A2  SOD2  SORBS1  SOX13  SPINK1  SREBF1  TAP1  TBXA2R  TCF1  TCF2  TFAM  TGFB1  TGIF  TH  THRSP  TIM3  TNF  TNFRSF6  TNFRSF8  TNFSF10  TRB3  TUB  TULP2  UBB  UCN  UCP2  UCP3  VDR  VEGF  WFS1  WFS2
ABDOMINAL AORTIC ANEURYSM  ABDOMINAL OBESITY-METABOLIC SYNDROME  ACANTHOSIS NIGRICANS  ACERULOPLASMINEMIA  ACRORENOOCULAR SYNDROME  AD  AHO  AIS  ALANINURIA WITH MICROCEPHALY, DWARFISM, ENAMEL HYPOPLASIA, AND DIABETES MELLITUS  ALMS  ANEMIA, SIDEROBLASTIC, X-LINKED  ANEURYSM, INTRACRANIAL BERRY  APOLIPOPROTEIN C-II DEFICIENCY  AREDYLD  ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA  ASPIRIN RESISTANCE  AT  ATHEROSCLEROSIS, PREMATURE, WITH DEAFNESS, NEPHROPATHY, DIABETES MELLITUS, PHOTOMYOCLONUS, AND DEGENERATIVE NEUROLOGIC DISEASE  AUTOIMMUNE DISEASE  AUTOIMMUNE POLYENDOCRINOPATHY SYNDROME, TYPE I  AUTOIMMUNE THYROID DISEASE, SUSCEPTIBILITY TO, 1  BBS  BILE AND PANCREATIC DUCTS, COMPLETE ABSENCE OF  BIRD-HEADED DWARFISM WITH PROGRESSIVE ATAXIA, INSULIN-RESISTANT DIABETES, GOITER, AND PRIMARY GONADAL INSUFFICIENCY  BLM  BRACHYDACTYLY, TYPE A2, WITH MICROCEPHALY  BSCL  BWS  CARCINOID TUMORS, INTESTINAL  CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY  CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA, COMBINED  CIRRHOSIS, FAMILIAL  CLEFT-LIMB-HEART MALFORMATION SYNDROME  CMT1B  CMT2B  COLLAGENOSIS, FAMILIAL REACTIVE PERFORATING  COMPLEMENT COMPONENT 2 DEFICIENCY  CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 1  CPAF  CRANIAL NERVES, RECURRENT PARESIS OF  CTNS  CURRARINO SYNDROME  DFNA6  DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL DOMINANT  DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL RECESSIVE  DIABETES INSIPIDUS, NEPHROGENIC, WITH MENTAL RETARDATION AND INTRACEREBRAL CALCIFICATION  DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED  DIABETES INSIPIDUS, NEUROHYPOPHYSEAL TYPE  DIABETES INSIPIDUS, NEUROHYPOPHYSEAL TYPE  DIABETES MELLITUS, CONGENITAL AUTOIMMUNE  DIABETES MELLITUS, INSULIN-DEPENDENT, 2  DIABETES MELLITUS, INSULIN-DEPENDENT, X-LINKED, SUSCEPTIBILITY TO  DIABETES MELLITUS, INSULIN-RESISTANT, WITH ACANTHOSIS NIGRICANS AND HYPERTENSION  DIABETES MELLITUS, NEONATAL-ONSET  DIABETES MELLITUS, NONINSULIN-DEPENDENT, 3  DIABETES MELLITUS, NONINSULIN-DEPENDENT, 4  DIABETES MELLITUS, TRANSIENT NEONATAL  DIABETES-DEAFNESS SYNDROME, MATERNALLY TRANSMITTED  DIABETIC NEPHROPATHY, SUSCEPTIBILITY TO  DIARRHEA, CHRONIC, WITH VILLOUS ATROPHY  DKC  DUPUYTREN CONTRACTURE  DYSTROPHIA MYOTONICA 1  EDEMA, FAMILIAL IDIOPATHIC, PREPUBERTAL  EEC3  EHLERS-DANLOS SYNDROME, TYPE VIII  ENDOMETRIAL CANCER  EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS  FA  FANCONI RENOTUBULAR SYNDROME  FASTING GLUCOSE AND SPECIFIC INSULIN LEVELS  FBS  FFS  FPLD  FRDA  FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA  FSGS1  GALACTOKINASE DEFICIENCY  GCCD1  GCKD  GLUTAMIC ACID DECARBOXYLASE, BRAIN, MEMBRANE FORM  GLYS1  GOUT  GRAVES DISEASE  GROWTH FACTORS, COMBINED DEFECT OF  HASHIMOTO THYROIDITIS  HEPATIC ADENOMAS, FAMILIAL  HEPATITIS B VACCINE, RESPONSE TO  HFE4  HIDRADENITIS SUPPURATIVA, FAMILIAL  HOMOCYSTEINEMIA  HYPERLIPIDEMIA, TYPE VI  HYPERLIPOPROTEINEMIA, TYPE V  HYPEROSTOSIS FRONTALIS INTERNA  HYPERTENSION, ESSENTIAL  HYPERTRIGLYCERIDEMIA, FAMILIAL  HYPOALPHALIPOPROTEINEMIA, PRIMARY  HYPOGONADISM, DIABETES MELLITUS, ALOPECIA, MENTAL RETARDATION, AND ELECTROCARDIOGRAPHIC ABNORMALITIES  HYPOPITUITARISM, CONGENITAL, WITH CENTRAL DIABETES INSIPIDUS  HYPOPROTEINEMIA, HYPERCATABOLIC  HYPOTENSION, ORTHOSTATIC  IBD1  ICHTHYOSIS AND MALE HYPOGONADISM  INSULIN RECEPTORS, FAMILIAL INCREASE IN  IPEX  IRON OVERLOAD IN AFRICA  ISLET CELL ADENOMATOSIS  KSS  LANGERHANS CELL HISTIOCYTOSIS  LDHCP  LEPRECHAUNISM  LIPODYSTROPHY, PARTIAL, WITH RIEGER ANOMALY, SHORT STATURE, AND INSULINOPENIC DIABETES MELLITUS  MAD  MENTAL RETARDATION SYNDROME, BELGIAN TYPE  MG  MICROTIA-ANOTIA  MITOCHONDRIAL MYOPATHY, LIPID TYPE  MJD  MODY1  MODY2  MODY3  MODY4  MODY5  MODY6  MODY  MULIBREY NANISM  MULLERIAN APLASIA  MUSCULAR ATROPHY, ATAXIA, RETINITIS PIGMENTOSA, AND DIABETES MELLITUS  MUSCULAR ATROPHY, JUVENILE SPINAL  MYELOPEROXIDASE DEFICIENCY  MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION  NESIDIOBLASTOSIS OF PANCREAS  NEUROAXONAL DYSTROPHY, INFANTILE  NEUROPATHY, HEREDITARY MOTOR AND SENSORY, OKINAWA TYPE  NIDDM1  NIDDM  OBESITY AND ENDOCRINOPATHY DUE TO IMPAIRED PROCESSING OF PROHORMONES  OBESITY  PANCREAS, DORSAL, AGENESIS OF  PANCREATIC AGENESIS, CONGENITAL  PANCREATIC BETA CELL AGENESIS WITH NEONATAL DIABETES MELLITUS  PANCREATIC CARCINOMA  PANCREATIC HYPOPLASIA, CONGENITAL, WITH DIABETES MELLITUS AND CONGENITAL HEART DISEASE  PATTERSON PSEUDOLEPRECHAUNISM SYNDROME  PCOS1  PCTT  PEARSON MARROW-PANCREAS SYNDROME  PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY  PHENFORMIN 4-HYDROXYLATION  PHOTOMYOCLONUS, DIABETES MELLITUS, DEAFNESS, NEPHROPATHY, AND CEREBRAL DYSFUNCTION  PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES  PITUITARY DWARFISM I  POLYHYDRAMNIOS, CHRONIC IDIOPATHIC  PREAXIAL HALLUCAL POLYDACTYLY  PREMATURE AGING SYNDROME, OKAMOTO TYPE  PROTEUS SYNDROME  PSEUDOACROMEGALY WITH SEVERE INSULIN RESISTANCE  PWS  PYOGENIC STERILE ARTHRITIS, PYODERMA GANGRENOSUM, AND ACNE  RAMON SYNDROME  RENAL TUBULOPATHY, DIABETES MELLITUS, AND CEREBELLAR ATAXIA DUE TO DUPLICATION OF MITOCHONDRIAL DNA  RETINITIS PIGMENTOSA, DEAFNESS, MENTAL RETARDATION, AND HYPOGONADISM  RETINOHEPATOENDOCRINOLOGIC SYNDROME  SCA6  SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME  SCHMIDT SYNDROME  SENIOR-LOKEN SYNDROME  SEPTOOPTIC DYSPLASIA  SHORT SYNDROME  SICKLE CELL ANEMIA  SJOGREN SYNDROME  SPINA BIFIDA  SPLENOPORTAL VASCULAR ANOMALIES  STIFF MAN SYNDROME, HEREDITARY FORM OF  STROKE  SUPERIOR TRANSVERSE SCAPULAR LIGAMENT, CALCIFICATION OF, FAMILIAL  TRMA  VITAMIN D-RESISTANT RICKETS WITH END-ORGAN UNRESPONSIVENESS TO 1,25-DIHYDROXYCHOLECALCIFEROL  WOLFRAM SYNDROME, MITOCHONDRIAL FORM  WOLFRAM SYNDROME  WRN