Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the hand (HP:0001155)help
Parent Node:
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Abnormality of finger (HP:0001167)help
Parent Node:
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Deviation of the hand or of fingers of the hand (HP:0009484)help
..Starting node
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Deviation of finger (HP:0004097)help
Term ID: 4097
Name: Deviation of finger
Synonym: Atypical position of finger; Deviated fingers; Finger pointing in a different direction than usual
Definition: Deviated fingers is a term that should be used if one or more fingers of the hand are deviated from their normal position, either to the radial or ulnar side. A deviation of a finger can be caused by an abnormal form of one or more of the phalanges of the affected finger, or by a deviation or displacement of one or more phalanges.
Comments:
Reference: HP:0004097
Genes and Diseases:
 
       Child Nodes:
........expandDeviation of the 5th finger (HP:0009179) help
................... HP:0004209 Clinodactyly of the 5th finger
................... HP:0009180 Ulnar deviation of the 5th finger
................... HP:0040020 Radial deviation of the 5th finger
........expandDeviation of the 4th finger (HP:0009273) help
................... HP:0009278 Ulnar deviation of the 4th finger
................... HP:0009279 Radial deviation of the 4th finger
................... HP:0040025 Clinodactyly of the 4th finger
........expandDeviation of the 3rd finger (HP:0009317) help
................... HP:0009462 Radial deviation of the 3rd finger
................... HP:0009463 Ulnar deviation of the 3rd finger
................... HP:0040024 Clinodactyly of the 3rd finger
........expandUlnar deviation of finger (HP:0009465) help
................... HP:0006156 Ulnar deviation of thumb
................... HP:0009180 Ulnar deviation of the 5th finger
................... HP:0009278 Ulnar deviation of the 4th finger
................... HP:0009463 Ulnar deviation of the 3rd finger
................... HP:0009464 Ulnar deviation of the 2nd finger
........expandRadial deviation of finger (HP:0009466) help
................... HP:0001234 Hitchhiker thumb
................... HP:0009279 Radial deviation of the 4th finger
................... HP:0009462 Radial deviation of the 3rd finger
................... HP:0009467 Radial deviation of the 2nd finger
................... HP:0040020 Radial deviation of the 5th finger
................... HP:0040021 Radial deviation of the thumb
........expandDeviation of the 2nd finger (HP:0009468) help
................... HP:0009464 Ulnar deviation of the 2nd finger
................... HP:0009467 Radial deviation of the 2nd finger
................... HP:0040022 Clinodactyly of the 2nd finger
........expandDeviation of the thumb (HP:0009603) help
................... HP:0001234 Hitchhiker thumb
................... HP:0009622 Distally placed thumb
................... HP:0009623 Proximal placement of thumb
................... HP:0040021 Radial deviation of the thumb
................... HP:0040023 Clinodactyly of the thumb
........expandOverlapping fingers (HP:0010557) help
........expandFinger clinodactyly (HP:0040019) help
................... HP:0004209 Clinodactyly of the 5th finger
................... HP:0040022 Clinodactyly of the 2nd finger
................... HP:0040023 Clinodactyly of the thumb
................... HP:0040024 Clinodactyly of the 3rd finger
................... HP:0040025 Clinodactyly of the 4th finger

 Sister Nodes: 
..expandRadial deviation of the hand or of fingers of the hand (HP:0009485) help
..expandUlnar deviation of the hand or of fingers of the hand (HP:0001193) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0004097HP:0004097Deviation of finger0GDF5 CL E G H8200228900Fibular hypoplasia and complex brachydactyly228900C1856738OMIM159984220601146
HP:0004097HP:0004097Deviation of finger0IKBKG CL E G H8517464Achromatopsia incomplete X-linkedCN036572ORPHA11512955961300248
HP:0004097HP:0004097Deviation of finger0PIEZO2 CL E G H638951154Cataract mental retardation hypogonadismORPHA13232926270613629
HP:0004097HP:0004097Deviation of finger0SOST CL E G H50964269500Sclerosteosis 1269500CN032489OMIM1177013771605740
HP:0004097HP:0004097Deviation of finger1GDF5 CL E G H8200228900Fibular hypoplasia and complex brachydactyly228900C1856738OMIM159984220601146
HP:0004097HP:0004097Deviation of finger1IKBKG CL E G H8517464Achromatopsia incomplete X-linkedCN036572ORPHA11512955961300248
HP:0004097HP:0004097Deviation of finger1PIEZO2 CL E G H638951154Cataract mental retardation hypogonadismORPHA13232926270613629
HP:0004097HP:0004097Deviation of finger1SOST CL E G H50964269500Sclerosteosis 1269500CN032489OMIM1177013771605740
HP:0004097HP:0004097Deviation of finger2GDF5 CL E G H8200228900Fibular hypoplasia and complex brachydactyly228900C1856738OMIM159984220601146
HP:0004097HP:0004097Deviation of finger2IKBKG CL E G H8517464Achromatopsia incomplete X-linkedCN036572ORPHA11512955961300248
HP:0004097HP:0004097Deviation of finger2PIEZO2 CL E G H638951154Cataract mental retardation hypogonadismORPHA13232926270613629
HP:0004097HP:0004097Deviation of finger2SOST CL E G H50964269500Sclerosteosis 1269500CN032489OMIM1177013771605740
HP:0004097HP:0004097Deviation of finger3GDF5 CL E G H8200228900Fibular hypoplasia and complex brachydactyly228900C1856738OMIM159984220601146
HP:0004097HP:0004097Deviation of finger3IKBKG CL E G H8517464Achromatopsia incomplete X-linkedCN036572ORPHA11512955961300248
HP:0004097HP:0004097Deviation of finger3PIEZO2 CL E G H638951154Cataract mental retardation hypogonadismORPHA13232926270613629
HP:0004097HP:0004097Deviation of finger3SOST CL E G H50964269500Sclerosteosis 1269500CN032489OMIM1177013771605740
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0004097HP:0004097Deviation of finger0HPGD CL E G H32481525ORPHA0181455154601688
HP:0004097HP:0004097Deviation of finger1HPGD CL E G H32481525ORPHA0181455154601688
HP:0004097HP:0004097Deviation of finger2HPGD CL E G H32481525ORPHA0181455154601688
HP:0004097HP:0004097Deviation of finger3HPGD CL E G H32481525ORPHA0181455154601688


Genes (339) :A2ML1 ABCC8 ABL1 ACVR1 AKT1 ALX1 ALX3 AMER1 AMMECR1 ANKRD11 ARID1B ASXL1 ATR ATRIP ATRX B3GLCT BAZ1B BBS1 BCOR BCR BHLHA9 BICD2 BLM BMP2 BMP4 BMPR1B BRAF BRAT1 BRCA1 BRCA2 BRIP1 BUB1 BUB1B BUB3 C12ORF57 CANT1 CCDC8 CCNQ CD96 CDC42 CDC45 CDC6 CDKL5 CDT1 CENPE CENPJ CEP152 CEP55 CEP57 CHD7 CHRNA7 CHST11 CHST3 CHSY1 CITED2 CKAP2L CLCF1 CLIP2 CNTN1 COG7 COL11A1 CPLANE1 CREBBP CRIPT CRKL CRLF1 CTU2 CUL4B CUL7 DACT1 DEAF1 DHCR7 DLX3 DONSON DPAGT1 DSP DVL1 DVL3 DYM EBP EFNB1 EFTUD2 EIF4A3 ELN EMG1 EP300 ERCC4 ESCO2 EVC EVC2 EZH2 FANCA FANCB FANCC FANCD2 FANCE FANCF FANCG FANCI FANCL FANCM FBN2 FGD1 FGF10 FGFR2 FGFR3 FLII FLNA FLNB FOXG1 FZD2 GABBR2 GABRD GATA4 GATA5 GATA6 GCK GDF1 GDF5 GJA1 GJA5 GMNN GPC3 GPC4 GTF2I GTF2IRD1 H19 HDAC4 HDAC8 HERC2 HIC1 HMGA2 HOXA11 HOXA13 HOXD13 HPGD HRAS IFT122 IFT43 IFT52 IGF1 IGF1R IGF2 IHH IKBKG INS IPW IQSEC2 JAG1 KAT6B KCNAB2 KCNJ11 KCNJ2 KDM1A KIAA0753 KIAA1109 KIF7 KLF13 KLHL7 KMT2A KPTN KRAS L1CAM LEMD3 LIFR LIG4 LIMK1 LMBR1 LMNA LMX1B LONP1 LZTR1 MAD2L2 MAGEL2 MAP2K1 MAP3K7 MAPK1 MASP1 MBD5 MCTP2 MECOM MECP2 MED12 MGAT2 MKRN3 MKRN3-AS1 MKS1 MLXIPL MOGS MYBPC1 MYH3 MYMK NAA10 NALCN NDN NEK1 NEK9 NIPBL NKX2-5 NKX2-6 NOG NPAP1 NPR2 NRAS NSUN2 NTNG1 NXN OBSL1 OFD1 OPA3 ORC1 ORC4 ORC6 PAFAH1B1 PALB2 PAX3 PCNT PDE6D PDX1 PHGDH PI4KA PIEZO2 PIGH PIGL PIGN PIGS PIK3R1 PITX1 PLK4 PLXND1 PNPLA6 PPP2R1A PQBP1 PRDM16 PRKDC PTEN PTF1A PTH1R PTPN11 PTRH2 PUF60 PWAR1 PWRN1 RAB18 RAB23 RAB3GAP1 RAB3GAP2 RAD21 RAD51 RAD51C RAF1 RAI1 RASA2 RB1 RBBP8 RBM8A RERE REV3L RFC2 RFWD3 RIT1 RNF216 RNU4ATAC ROR2 RRAS RUNX2 SALL1 SAMD9 SATB2 SEMA3E SETBP1 SETD5 SF3B4 SH3PXD2B SHANK3 SHH SHOX SIM1 SIN3A SKI SLC26A2 SLC2A10 SLX4 SMAD4 SMC1A SMC3 SMOC1 SNORD115-1 SNORD116-1 SNRPB SNRPN SOS1 SOS2 SOST SPECC1L SRCAP STXBP1 TBC1D24 TBL2 TBX1 TBX15 TBX22 TBX4 TBX5 TCF4 TCTN3 TFAP2A TFAP2B TGDS TMEM216 TMEM94 TNNI2 TNNT3 TP63 TPM2 TRAIP TRAPPC9 TRIP13 TRPS1 TRPV4 TWIST1 UBA1 UBE2T UBE3A UBE3B UBR1 VPS13B WDR19 WDR35 WNT5A WNT7A XRCC2 XRCC4 XYLT1 YWHAE YY1AP1 ZC4H2 ZFPM2 ZIC3

Diseases (288) :228900 1525 464 1154 269500 606176 617602 306542 391474 136760 2332 148050 97297 301040 309580 209900 309800 261330 618291 93384 609441 163950 211750 618167 143095 272440 610313 612540 608779 2754 277170 272430 618142 857 818 3352 609638 180700 300960 3103 269000 268300 952 277590 121050 305400 93259 602849 1826 304120 176270 93406 3071 218330 608747 270450 616489 617822 601559 79474 617137 1596 616738 305450 249000 606056 1146 1147 2053 1358 2751 617022 186500 186570 615923 311200 300209 67036 1529 256520 616531 269880 616362 615966 609069 1387 268310 617053 798 154400 2632 613406 628 222600 139210 921 142900 2896 618316 113500 606835 228930 602531 648 79134 337 135100 744 300373 300990 261250 251056 808 210600 847 709 261540 904 568 2712 157801 609432 210900 93396 617877 112600 139471 607932 93388 616849 115150 618056 84 617883 1052 1777 1425 2616 140952 300707 1308 616737 2554 3095 613823 236500 138 199318 612001 605282 3303 3255 228520 180849 615789 85293 273750 819 270400 617604 86309 608093 3107 223800 35173 1520 304110 610536 268305 194050 1270 211180 193530 314390 915 149730 794 101400 90650 108721 272460 1606 251071 187500 3250 113100 2710 373 180860 1001 199 300882 531 94063 71289 605432 2438 140000 186000 1515 73272 112500 3047 170390 616728 200990 319182 605130 615637 2466 99812 235 3332 161200 600373 257920 228402 778 212066 122470 611377 1507 2750 224690 217385 2637 210720 376 618010 280000 2059 618143 1275 570 1173 309500 156400 616263 508488 614222 201000 1587 606744 3320 274000 2636 616651 1452 251019 137834 48652 606232 240 171829 94065 93307 56304 3342 300590 610759 1106 1393 117650 1519 2044 136140 79500 260660 261279 113620 46627 169100 616145 1388 1071 69085 1896 352530 77258 2635 1145 238446 244450 243800 193 3454 314580 257850
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.