Human Phenotype Ontology 
Grandparent Node:
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Abnormal posterior eye segment morphology (HP:0004329)help
Parent Node:
expand
Abnormal fundus morphology (HP:0001098)help
..Starting node
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Abnormal retinal morphology (HP:0000479)help
Term ID: 479
Name: Abnormal retinal morphology
Synonym: Abnormal retina; Abnormality of the retina; Anomaly of the retina; Retina issue; Retinal disease
Definition: A structural abnormality of the retina.
Comments:
Reference: HP:0000479
Genes and Diseases:
 
       Child Nodes:
........expandRetinal coloboma (HP:0000480) help
................... HP:0001116 Macular coloboma
................... HP:0007808 Bilateral retinal coloboma
................... HP:0031614 Inferior retinal coloboma
........expandRetinopathy (HP:0000488) help
................... HP:0500049 Retinopathy of prematurity
........expandAbnormal chorioretinal morphology (HP:0000532) help
................... HP:0000567 Chorioretinal coloboma
................... HP:0001135 Chorioretinal dystrophy
................... HP:0007661 Abnormality of chorioretinal pigmentation
................... HP:0007731 Chorioretinal dysplasia
................... HP:0007858 Chorioretinal lacunae
................... HP:0012424 Chorioretinitis
................... HP:0025567 Central serous chorioretinopathy
................... HP:0200065 Chorioretinal degeneration
........expandRetinal detachment (HP:0000541) help
................... HP:0007899 Retinal nonattachment
................... HP:0007917 Tractional retinal detachment
................... HP:0007929 Peripheral retinal detachment
................... HP:0012230 Rhegmatogenous retinal detachment
................... HP:0012231 Exudative retinal detachment
........expandRetinal degeneration (HP:0000546) help
................... HP:0000547 Tapetoretinal degeneration
................... HP:0000608 Macular degeneration
................... HP:0000655 Vitreoretinal degeneration
................... HP:0001105 Retinal atrophy
................... HP:0007769 Peripheral retinal degeneration
................... HP:0008020 Progressive cone degeneration
................... HP:0008035 Retinitis pigmentosa inversa
........expandRetinal dystrophy (HP:0000556) help
................... HP:0000510 Rod-cone dystrophy
................... HP:0000548 Cone/cone-rod dystrophy
................... HP:0001135 Chorioretinal dystrophy
................... HP:0007642 Congenital stationary night blindness
................... HP:0007754 Macular dystrophy
................... HP:0007963 Pattern dystrophy of the retina
................... HP:0030635 Retinal dystrophy with early macular involvement
........expandRetinal hemorrhage (HP:0000573) help
................... HP:0025243 Subretinal hemorrhage
................... HP:0025244 Subretinal pigment epithelium hemorrhage
................... HP:0025574 Macular hemmorhage
................... HP:0031611 Sub-inner limiting membrane hemorrhage
................... HP:0031805 Intraretinal hemorrhage
........expandAngioid streaks of the fundus (HP:0001102) help
........expandAbnormal macular morphology (HP:0001103) help
................... HP:0000493 Abnormal foveal morphology
................... HP:0000608 Macular degeneration
................... HP:0001116 Macular coloboma
................... HP:0007754 Macular dystrophy
................... HP:0008002 Abnormality of macular pigmentation
................... HP:0008059 Aplasia/Hypoplasia of the macula
................... HP:0011506 Choroidal neovascularization
................... HP:0011508 Macular hole
................... HP:0025574 Macular hemmorhage
................... HP:0030495 Abnormality of macular vasculature
................... HP:0030498 Macular thickening
................... HP:0030500 Yellow/white lesions of the macula
................... HP:0031150 Vitreomacular adhesion
................... HP:0031151 Vitreomacular traction
........expandAbnormality of retinal pigmentation (HP:0007703) help
................... HP:0000580 Pigmentary retinopathy
................... HP:0007814 Retinal pigment epithelial mottling
........expandRetinal infarction (HP:0007866) help
........expandHypermyelinated retinal nerve fibers (HP:0007922) help
........expandRetinal dysplasia (HP:0007973) help
........expandAbnormality of the retinal vasculature (HP:0008046) help
................... HP:0000630 Abnormal retinal artery morphology
................... HP:0000660 Lipemia retinalis
................... HP:0001095 Hypertensive retinopathy
................... HP:0007685 Peripheral retinal avascularization
................... HP:0007763 Retinal telangiectasia
................... HP:0007797 Retinal vascular malformation
................... HP:0007815 Abnormal distribution of retinal arterioles and venules
................... HP:0007843 Attenuation of retinal blood vessels
................... HP:0007850 Retinal vascular proliferation
................... HP:0007986 Increased retinal vascularity
................... HP:0012636 Retinal vein occlusion
................... HP:0012841 Retinal vascular tortuosity
................... HP:0025188 Retinal vasculitis
................... HP:0030666 Retinal neovascularization
........expandRetinal fold (HP:0008052) help
................... HP:0001493 Falciform retinal fold
........expandAplasia/Hypoplasia of the retina (HP:0008061) help
................... HP:0007770 Hypoplasia of the retina
................... HP:0008059 Aplasia/Hypoplasia of the macula
................... HP:0010728 Aplasia of the retina
........expandRetinal hamartoma (HP:0009594) help
................... HP:0009711 Retinal capillary hemangioma
................... HP:0012778 Retinal astrocytic hamartoma
................... HP:0030508 Retinal cavernous hemangioma
................... HP:0030509 Retinal racemose hemangioma
................... HP:0030510 Combined hamartoma of the retinal pigment epithelium and retina
........expandRetinal perforation (HP:0011958) help
................... HP:0011508 Macular hole
................... HP:0011530 Retinal hole
........expandRetinal neoplasm (HP:0012777) help
................... HP:0009919 Retinoblastoma
........expandRetinal thinning (HP:0030329) help
........expandRetinoschisis (HP:0030502) help
................... HP:0012152 Foveoschisis
........expandYellow/white lesions of the retina (HP:0030506) help
................... HP:0001147 Retinal exudate
................... HP:0007862 Retinal calcification
................... HP:0011510 Drusen
................... HP:0012045 Retinal flecks
................... HP:0030500 Yellow/white lesions of the macula
................... HP:0030507 Retinal crystals
................... HP:0030643 Vitelliform-like retinal lesions
................... HP:0031606 Retinal cotton wool spot
........expandSubretinal fluid (HP:0031526) help
........expandIntraretinal fluid (HP:0031527) help
........expandSubretinal deposits (HP:0031528) help
................... HP:0031529 Focal subretinal deposits
................... HP:0031530 Multifocal subretinal deposits
........expandSub-RPE deposits (HP:0031531) help
................... HP:0031532 Focal sub-RPE deposits
................... HP:0031533 Multifocal sub-RPE deposits

 Sister Nodes: 
..expandAbnormal choroid morphology (HP:0000610) help
..expandAbnormality of fundus pigmentation (HP:0031605) help
..expandAbnormality of the optic nerve (HP:0000587) help
..expandAplasia/Hypoplasia affecting the fundus (HP:0008057) help
..expandFundus atrophy (HP:0001099) help
..expandFundus hemorrhage (HP:0031803) help
..expandMizuo phenomenon (HP:0030824) help
..expandOcular albinism (HP:0001107) help
..expandTapetal-like fundal reflex (HP:0025583) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0000479HP:0000479Abnormal retinal morphology0TMEM231 CL E G H79583614970Joubert syndrome 20614970C3554235OMIM11920237234614949
HP:0000479HP:0000479Abnormal retinal morphology1TMEM231 CL E G H79583614970Joubert syndrome 20614970C3554235OMIM11920237234614949
HP:0000479HP:0000479Abnormal retinal morphology2TMEM231 CL E G H79583614970Joubert syndrome 20614970C3554235OMIM11920237234614949
HP:0000479HP:0000479Abnormal retinal morphology3TMEM231 CL E G H79583614970Joubert syndrome 20614970C3554235OMIM11920237234614949
HP:0000479HP:0000479Abnormal retinal morphology4TMEM231 CL E G H79583614970Joubert syndrome 20614970C3554235OMIM11920237234614949
HP:0000479HP:0000479Abnormal retinal morphology5TMEM231 CL E G H79583614970Joubert syndrome 20614970C3554235OMIM11920237234614949
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0000479HP:0000479Abnormal retinal morphology0KRT25 CL E G H147183170ORPHA042630839616646
HP:0000479HP:0000479Abnormal retinal morphology0KRT71 CL E G H112802170ORPHA015228927608245
HP:0000479HP:0000479Abnormal retinal morphology0KRT74 CL E G H121391170ORPHA048528929608248
HP:0000479HP:0000479Abnormal retinal morphology0LIPH CL E G H200879170ORPHA0317118483607365
HP:0000479HP:0000479Abnormal retinal morphology0LPAR6 CL E G H10161170ORPHA0269315520609239
HP:0000479HP:0000479Abnormal retinal morphology0POLG CL E G H5428254886ORPHA030014389179174763
HP:0000479HP:0000479Abnormal retinal morphology0TK2 CL E G H7084254886ORPHA06022811831188250
HP:0000479HP:0000479Abnormal retinal morphology1KRT25 CL E G H147183170ORPHA042630839616646
HP:0000479HP:0000479Abnormal retinal morphology1KRT71 CL E G H112802170ORPHA015228927608245
HP:0000479HP:0000479Abnormal retinal morphology1KRT74 CL E G H121391170ORPHA048528929608248
HP:0000479HP:0000479Abnormal retinal morphology1LIPH CL E G H200879170ORPHA0317118483607365
HP:0000479HP:0000479Abnormal retinal morphology1LPAR6 CL E G H10161170ORPHA0269315520609239
HP:0000479HP:0000479Abnormal retinal morphology1POLG CL E G H5428254886ORPHA030014389179174763
HP:0000479HP:0000479Abnormal retinal morphology1TK2 CL E G H7084254886ORPHA06022811831188250
HP:0000479HP:0000479Abnormal retinal morphology2KRT25 CL E G H147183170ORPHA042630839616646
HP:0000479HP:0000479Abnormal retinal morphology2KRT71 CL E G H112802170ORPHA015228927608245
HP:0000479HP:0000479Abnormal retinal morphology2KRT74 CL E G H121391170ORPHA048528929608248
HP:0000479HP:0000479Abnormal retinal morphology2LIPH CL E G H200879170ORPHA0317118483607365
HP:0000479HP:0000479Abnormal retinal morphology2LPAR6 CL E G H10161170ORPHA0269315520609239
HP:0000479HP:0000479Abnormal retinal morphology2POLG CL E G H5428254886ORPHA030014389179174763
HP:0000479HP:0000479Abnormal retinal morphology2TK2 CL E G H7084254886ORPHA06022811831188250
HP:0000479HP:0000479Abnormal retinal morphology3KRT25 CL E G H147183170ORPHA042630839616646
HP:0000479HP:0000479Abnormal retinal morphology3KRT71 CL E G H112802170ORPHA015228927608245
HP:0000479HP:0000479Abnormal retinal morphology3KRT74 CL E G H121391170ORPHA048528929608248
HP:0000479HP:0000479Abnormal retinal morphology3LIPH CL E G H200879170ORPHA0317118483607365
HP:0000479HP:0000479Abnormal retinal morphology3LPAR6 CL E G H10161170ORPHA0269315520609239
HP:0000479HP:0000479Abnormal retinal morphology3POLG CL E G H5428254886ORPHA030014389179174763
HP:0000479HP:0000479Abnormal retinal morphology3TK2 CL E G H7084254886ORPHA06022811831188250
HP:0000479HP:0000479Abnormal retinal morphology4KRT25 CL E G H147183170ORPHA042630839616646
HP:0000479HP:0000479Abnormal retinal morphology4KRT71 CL E G H112802170ORPHA015228927608245
HP:0000479HP:0000479Abnormal retinal morphology4KRT74 CL E G H121391170ORPHA048528929608248
HP:0000479HP:0000479Abnormal retinal morphology4LIPH CL E G H200879170ORPHA0317118483607365
HP:0000479HP:0000479Abnormal retinal morphology4LPAR6 CL E G H10161170ORPHA0269315520609239
HP:0000479HP:0000479Abnormal retinal morphology4POLG CL E G H5428254886ORPHA030014389179174763
HP:0000479HP:0000479Abnormal retinal morphology4TK2 CL E G H7084254886ORPHA06022811831188250
HP:0000479HP:0000479Abnormal retinal morphology5KRT25 CL E G H147183170ORPHA042630839616646
HP:0000479HP:0000479Abnormal retinal morphology5KRT71 CL E G H112802170ORPHA015228927608245
HP:0000479HP:0000479Abnormal retinal morphology5KRT74 CL E G H121391170ORPHA048528929608248
HP:0000479HP:0000479Abnormal retinal morphology5LIPH CL E G H200879170ORPHA0317118483607365
HP:0000479HP:0000479Abnormal retinal morphology5LPAR6 CL E G H10161170ORPHA0269315520609239
HP:0000479HP:0000479Abnormal retinal morphology5POLG CL E G H5428254886ORPHA030014389179174763
HP:0000479HP:0000479Abnormal retinal morphology5TK2 CL E G H7084254886ORPHA06022811831188250


Genes (734) :AARS ABCA4 ABCC6 ABCC8 ABHD12 ACD ACO2 ACOX1 ACTA2 ACTB ACTG1 ACVRL1 ADAM9 ADAMTS18 ADAMTSL1 ADAMTSL4 ADAR ADGRV1 AGBL5 AGXT AHI1 AHR AIPL1 AIRE AKT1 ALDH1A3 ALDH3A2 ALMS1 AMACR ANK1 ANO10 AP3B2 AP3D1 AP5Z1 APC APOB APOC2 APOE ARHGEF18 ARL13B ARL2BP ARL3 ARL6 ARL6IP6 ARMC9 ARV1 ARVCF ASAH1 ASXL1 ATF6 ATOH7 ATP1A2 ATP6 ATP6V0A2 ATP6V1A ATP6V1E1 ATP8 ATXN2 ATXN7 B3GALNT2 B3GLCT B4GAT1 B9D1 B9D2 BAP1 BAZ1B BBIP1 BBS1 BBS10 BBS12 BBS2 BBS4 BBS5 BBS7 BBS9 BCOR BCS1L BEST1 BLOC1S3 BMP4 BRAF C12ORF57 C1QTNF5 C2CD3 C4A C8ORF37 CA4 CABP4 CACNA1A CACNA1F CACNA2D4 CAPN5 CASK CAV1 CBS CC2D2A CCDC22 CCM2 CCNQ CCR1 CDH23 CDH3 CDHR1 CDK4 CDKN2A CDKN2B CDKN2D CENPF CEP120 CEP164 CEP290 CEP41 CEP55 CEP78 CEP83 CERKL CFAP410 CFH CHD7 CHEK2 CHM CHN1 CHRDL1 CHST14 CHST6 CIB2 CLCN2 CLCNKB CLDN19 CLIP2 CLN3 CLN5 CLN6 CLRN1 CLTC CNGA1 CNGA3 CNGB1 CNGB3 CNKSR2 CNNM4 COA7 COA8 COL11A1 COL18A1 COL1A1 COL25A1 COL2A1 COL4A1 COL5A1 COL5A2 COL9A1 COL9A2 COL9A3 COMT COQ2 COX1 COX10 COX14 COX15 COX2 COX20 COX3 COX6B1 COX7B COX8A CP CRB1 CREBBP CRPPA CRX CRYAB CSPP1 CTC1 CTLA4 CTNNA1 CTNNB1 CTNS CTSA CTSD CWC27 CYFIP2 CYP1B1 CYP4V2 CYSLTR2 CYTB DACT1 DAG1 DEAF1 DGCR2 DGCR6 DGCR8 DHDDS DHX38 DNAJC21 DNM1 DNM2 DPM1 DPP6 DRAM2 DUX4 DYNC2H1 DYNC2LI1 ECHS1 EDN3 EDNRB EEF1A2 EFEMP1 ELMO2 ELN ELOVL4 ENG ENPP1 EP300 EPG5 ERAP1 ERCC1 ERCC2 ERCC3 ERCC4 ERCC5 ERCC6 ERCC8 ESS2 ETHE1 EXOSC2 EXOSC3 EYS FAM111A FAM161A FAS FASTKD2 FBLN5 FBN1 FBN2 FDXR FGF12 FGF3 FGFR1 FGFR2 FH FKRP FKTN FLCN FLII FLNB FLVCR1 FOXC1 FOXE3 FOXRED1 FRG1 FSCN2 FTL FZD4 G6PC GABRB2 GALNT3 GATA3 GBA GCDH GCK GDF2 GDF3 GDF6 GGCX GLB1 GM2A GNA11 GNAQ GNAT1 GNAT2 GNB3 GNB5 GNPTAB GP1BB GPIHBP1 GPR143 GPR179 GRIN2D GRK1 GRM6 GRN GSS GTF2I GTF2IRD1 GUCA1A GUCA1B GUCY2D GZF1 HACE1 HADH HADHA HADHB HBB HCCS HCN1 HEXA HEXB HFE HGSNAT HHAT HIRA HK1 HLA-A HLA-B HLA-DPA1 HLA-DPB1 HMX1 HPS4 HPS5 HPS6 HSD11B2 HSD17B10 HSPD1 IDH3B IDS IDUA IFT122 IFT140 IFT172 IFT27 IFT74 IFT80 IFT88 IGFBP7 IKBKG IL10 IL12A IL12A-AS1 IL12B IL23R IMPDH1 IMPG1 IMPG2 INPP5E INS INVS IQCB1 IQSEC2 ITM2B JAG1 JMJD1C KCNA2 KCNB1 KCNJ11 KCNJ13 KCNV2 KIAA0586 KIAA1549 KIF11 KIF1B KIZ KLHL7 KLRC4 KRAS KRIT1 KRT25 KRT71 KRT74 LAMA1 LARGE1 LCA5 LETM1 LIMK1 LIPH LIPT1 LMF1 LMNA LPAR6 LPL LRAT LRIT3 LRP2 LRP5 LTBP2 LYST LZTFL1 MAF MAFB MAK MAN2B1 MAPKAPK3 MAPRE2 MAX MC1R MCOLN1 MDH2 MEFV MERTK MFRP MFSD8 MGMT MIR204 MITF MKKS MKS1 MLX MLXIPL MMACHC MPDZ MSTO1 MTFMT MTTP MVK MYD88 MYO5A MYO6 MYO7A MYOC NAA10 ND1 ND2 ND4 ND4L ND5 ND6 NDP NDUFA10 NDUFA12 NDUFA13 NDUFA2 NDUFA4 NDUFA9 NDUFAF1 NDUFAF2 NDUFAF5 NDUFAF6 NDUFB11 NDUFS1 NDUFS2 NDUFS3 NDUFS4 NDUFS7 NDUFS8 NDUFV1 NDUFV2 NECAP1 NEK1 NEK2 NELFA NEU1 NF2 NHS NMNAT1 NOD2 NOTCH3 NPHP1 NPHP3 NPHP4 NR2E3 NRL NSD2 NSMCE2 NTRK2 NUS1 NYX OAT OCA2 OCRL OFD1 OPA1 OPN1LW OPN1MW OTX2 P3H2 PANK2 PAX2 PAX6 PCARE PCDH15 PCYT1A PDCD10 PDE6A PDE6B PDE6C PDE6D PDE6G PDE6H PDHA1 PDX1 PDZD7 PEPD PET100 PEX1 PEX10 PEX11B PEX12 PEX13 PEX14 PEX16 PEX19 PEX2 PEX26 PEX3 PEX5 PEX6 PEX7 PGAP1 PGK1 PHYH PIEZO2 PIGL PIK3CA PITPNM3 PITX3 PLK4 PLOD1 PMM2 PMPCA PNPLA6 POC1B POGZ POLG POMGNT1 POMGNT2 POMK POMT1 POMT2 PORCN POT1 POU3F4 PPP3CA PPT1 PRCD PRDM5 PRDX1 PROM1 PROS1 PRPF3 PRPF31 PRPF4 PRPF6 PRPF8 PRPH2 PRPS1 PRRT2 PRSS56 PRTN3 PTCH1 PTEN PTPN22 PUF60 RAB18 RAB28 RAB3GAP1 RAB3GAP2 RAI1 RAX2 RB1 RBP3 RBP4 RCBTB1 RD3 RDH11 RDH12 RDH5 REEP6 RET RFC2 RGR RHO RIMS1 RLBP1 RMRP RNASEH1 RNF113A RNF216 RNU4ATAC ROM1 RP1 RP1L1 RP2 RP9 RPE65 RPGR RPGRIP1 RPGRIP1L RPS6KA3 RREB1 RRM2B RS1 RXYLT1 SACS SAG SALL1 SALL4 SAR1B SCAPER SCN1A SCN3A SCN8A SCO1 SDCCAG8 SDHA SDHAF1 SDHAF2 SDHB SDHC SDHD SEC24C SEMA3E SEMA4A SF3B1 SH2B1 SH3BP2 SHH SIX6 SLC12A6 SLC13A5 SLC19A2 SLC19A3 SLC1A2 SLC24A1 SLC24A5 SLC25A15 SLC35A2 SLC37A4 SLC38A8 SLC45A2 SLC52A2 SLC52A3 SLC7A14 SMAD4 SMCHD1 SMPD1 SNRNP200 SOX10 SPATA7 SPG11 STAT3 STAT4 STN1 STUB1 STXBP1 SUMF1 SURF1 SYCE1 SYNGAP1 SYNJ1 SZT2 TACO1 TBC1D20 TBL2 TBX1 TBX22 TCTN2 TEAD1 TEK TENM3 TERF2IP TERT TFAP2A TIMP3 TINF2 TK2 TLR4 TMCO1 TMEM107 TMEM127 TMEM138 TMEM216 TMEM231 TMEM237 TMEM67 TMEM98 TNFRSF11A TNFRSF11B TOPORS TPP1 TRAF3IP1 TRAK1 TRAPPC9 TREX1 TRIM32 TRIM37 TRIM44 TRNE TRNF TRNH TRNK TRNL1 TRNN TRNQ TRNS1 TRNS2 TRNT1 TRNW TRPM1 TSC1 TSC2 TSPAN12 TTC21B TTC8 TTLL5 TTPA TUB TUBB TUBB4B TUBGCP4 TUBGCP6 TULP1 TXN2 TYR UBA5 UBAC2 UBE3B UFD1 UNC119 USH1C USH1G USH2A VCAN VHL VPS13B WARS2 WASHC5 WDPCP WDR19 WDR34 WDR60 WFS1 WHRN WRN WT1 WWOX XRCC4 XYLT2 YAP1 YWHAG ZFYVE26 ZNF408 ZNF423 ZNF469 ZNF513

Diseases (719) :170 254886 614970 442835 791 1872 827 758 264800 177850 99885 618 614559 613834 2995 521445 225200 259900 220493 608629 65 744 615109 615113 816 270200 64 251066 306511 613647 873 615558 158029 1556 617622 617020 97297 221900 551500 480 899 615181 261540 615287 564 39044 209900 615981 615982 2712 300166 613194 153700 193220 139471 607932 99872 605670 615948 117 617406 300476 193235 394 2318 1897 474 3156 614845 610188 614464 615862 617547 602271 214800 180 309300 601776 615651 607364 2196 256731 601780 1871 1873 90654 250984 560 154780 604841 1571 267750 287 93346 94068 166011 485 90653 132450 156550 183900 108300 611773 607595 180000 614284 550 2556 48818 614643 613763 397715 615636 900 617572 219900 219800 98976 210370 616538 819 617052 615368 608799 616502 269 897 126600 3019 1493 1466 220295 602473 614678 3437 2833 154700 2791 2396 613153 236670 253800 272 122 272460 83461 157846 90050 133780 211900 25 91135 610842 3205 617173 252600 614706 617662 464282 616756 5 603903 465508 179 3287 300438 612572 309900 93473 607014 607016 218330 615630 464 308300 213300 610156 616079 616546 2526 152950 615960 613154 280 79474 222448 2143 2788 615994 610202 248500 2505 578 252650 35612 610951 617121 79282 200100 14 33226 79476 190 649 310600 305390 618234 263520 812 637 101000 627 90340 268100 436182 617253 616896 16 610125 614292 216873 234200 1475 120330 35737 120430 615665 742 912 44 614871 614877 614873 773 266500 615802 300653 108145 3474 280000 615108 2518 616171 1900 225400 1170 215470 1173 275400 253280 617123 614830 615249 613155 90354 743 615922 600059 613517 77301 2969 158350 508488 2510 182290 615147 617175 616108 612712 607475 607476 175 300953 1824 616651 611560 192 792 312700 615041 98 270550 607323 71 615993 613615 212550 1496 49827 249270 607616 585 272200 615145 113620 613990 617562 617563 614465 608091 610688 613550 2801 239000 204500 247691 192315 615988 225 805 538 613819 615860 96 616188 615771 617879 251270 613843 478029 616811 79434 892 193 614377 902 277700 616211 614322 85194 605822 1473 616468 614844 604116 601718 248200 612674 264470 243310 774 612775 615458 605472 604393 268000 240300 203800 614307 284289 617276 284804 207750 612291 615434 618173 110 600151 613575 49382 569 104 644 357074 183090 94147 164500 615995 615987 615989 616562 615983 615984 615986 568 309800 256000 124000 99000 611809 1777 218340 614500 600852 610427 215 300071 610478 163937 606721 1454 612285 7 140952 601067 1573 225280 601553 613660 243605 615991 610189 617236 608380 126700 138 259500 303100 233 217800 614869 248190 204200 614180 276902 613756 613767 217080 220110 436271 609508 73229 607426 255241 309801 600105 180849 120970 612199 608970 411629 610127 250410 857 192430 613861 618220 616311 600110 610651 133540 216400 51188 617763 602772 93325 127000 606068 608895 616118 617717 313855 29072 88628 609033 250923 158900 607921 232200 2237 613702 436274 610444 616389 444490 615947 614565 613411 257270 266130 602093 613827 601777 204000 71212 746 609016 609015 252930 616544 1422 612109 218030 100994 266920 616394 615996 617119 614224 180105 616151 616152 613581 609254 118450 610356 171300 615780 612943 116860 238600 613341 615058 601813 614181 617111 617339 613862 611040 616170 616722 605231 615990 277400 502423 617675 260920 33445 607821 276900 615565 608553 266900 606996 611131 613750 310500 534 300804 300424 303700 216866 607236 137902 120200 613428 602083 85167 608940 613810 163500 613801 613093 613582 610024 772 234580 601539 214100 266510 614866 614867 214110 614863 614879 600977 212065 1180 245800 615973 616364 613156 2092 305600 1435 256730 610599 608051 612657 612095 603786 601414 600138 613983 608161 169150 608133 311070 615374 613757 610381 1587 180200 615233 616428 610612 617304 613769 610445 613731 603649 329336 212840 180100 613587 312600 180104 204100 613794 304020 300834 300029 300455 608194 613826 258100 613758 107480 959 618195 3208 252011 610283 610282 261222 611638 613830 370097 300896 232220 97229 615725 610359 604360 617341 412057 616947 921 136900 602152 609923 616629 352530 253250 616084 613216 613310 615985 613464 616335 600132 2707 276904 606943 613809 276901 193300 216550 617710 614378 615633 222300 611383 100996 270700 616469 613617 41 567 333 228000 616517 904 1243 221061 172870 351 256540 194050 88632 230800 230500 309246 272800 268800 617460 614075 617781 214500 615219 256550 136 258870 613105 136880 238970 606574 257200 268130 213980 2752 615972 616959 143200 616307 600376 617433 535000 614077 178333 300600 613703 54 215500 614073 614074 103470 2751 186580 203200 106210 136520 118400 113750 609218 79435 108985 79431 203100
 

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