Human Phenotype Ontology 
Grandparent Node:
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Phenotypic abnormality (HP:0000118)help
Parent Node:
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Neoplasm (HP:0002664)help
..Starting node
..expand
Neoplasm by histology (HP:0011792)help
Term ID: 11792
Name: Neoplasm by histology
Synonym:
Definition: Neoplasm categorized according to type of histological abnormality.
Comments:
Reference: HP:0011792
Genes and Diseases:
 
       Child Nodes:
........expandMelanoma (HP:0002861) help
................... HP:0007716 Intraocular melanoma
................... HP:0012056 Cutaneous melanoma
........expandEmbryonal neoplasm (HP:0002898) help
................... HP:0002884 Hepatoblastoma
................... HP:0006743 Embryonal rhabdomyosarcoma
................... HP:0009792 Teratoma
................... HP:0009919 Retinoblastoma
................... HP:0011794 Embryonal renal neoplasm
........expandHamartoma (HP:0010566) help
................... HP:0001054 Numerous nevi
................... HP:0004390 Hamartomatous polyposis
................... HP:0008696 Renal hamartoma
................... HP:0009731 Cerebral hamartomata
................... HP:0010568 Hamartoma of the eye
................... HP:0011068 Odontoma
................... HP:0031111 Cutaneous hamartoma
................... HP:0100764 Lymphangioma
................... HP:0100882 Fibrous hamartoma
................... HP:0100883 Chorangioma
........expandFibrous tissue neoplasm (HP:0012316) help
................... HP:0010614 Fibroma
................... HP:0012315 Histiocytoma
................... HP:0025197 Inclusion body fibromatosis
........expandNervous tissue neoplasm (HP:0030060) help
................... HP:0030061 Neuroectodermal neoplasm
........expandEpithelial neoplasm (HP:0031492) help
................... HP:0030731 Carcinoma
................... HP:0031493 Glandular cell neoplasm
........expandSarcoma (HP:0100242) help
................... HP:0002669 Osteosarcoma
................... HP:0006765 Chondrosarcoma
................... HP:0008663 Renal sarcoma
................... HP:0012254 Ewing's sarcoma
................... HP:0030448 Soft tissue sarcoma

 Sister Nodes: 
..expandNeoplasm by anatomical site (HP:0011793) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011792HP:0011792Neoplasm by histology0 CL E G H
HP:0011792HP:0011792Neoplasm by histology1 CL E G H
HP:0011792HP:0011792Neoplasm by histology2 CL E G H
HP:0011792HP:0011792Neoplasm by histology3 CL E G H
HP:0011792HP:0011792Neoplasm by histology4 CL E G H
HP:0011792HP:0011792Neoplasm by histology5 CL E G H
HP:0011792HP:0011792Neoplasm by histology6 CL E G H
HP:0011792HP:0011792Neoplasm by histology7 CL E G H


Genes (245) :ABCA5 ACD ACTB ACVR1 ADAMTS3 AKT1 ALX4 ANTXR2 APC APC2 ASCL1 ASPSCR1 ATP6V1B2 AXIN2 BAP1 BARD1 BDNF BMPER BMPR1A BMPR1B BRAF BRCA1 BRCA2 BRD4 BRIP1 BUB1 BUB1B BUB3 C11ORF95 CCBE1 CDC73 CDK4 CDKN1A CDKN1B CDKN1C CDKN2A CDKN2B CDKN2C CDKN2D CEP57 CHEK2 COL18A1 COL1A1 COMP CPLANE1 CREB1 CTNNB1 CTSC CYSLTR2 DCC DDB2 DHCR24 DICER1 DIS3L2 DKC1 DLC1 DMRT3 DYNC2LI1 EDN3 ELMO2 EP300 EPCAM ERBB2 ERCC2 ERCC3 ERCC4 ERCC5 ERCC6 EWSR1 EXT1 EXT2 FAM20C FAN1 FAT4 FGF3 FGFR3 FH FIBP FLCN FLI1 FLNA FOXC2 FOXO1 GABRD GATA4 GDF5 GDNF GLI3 GNA11 GNAQ GNAS GPC3 GPC4 H19 H19-ICR HDAC4 HRAS IDH1 IDH2 IGF2 INHBA KCNAB2 KCNH1 KCNQ1 KCNQ1OT1 KEAP1 KIAA0753 KIF1B KIF7 KIT KLLN KRAS KRT1 KRT10 KRT17 LMNA LRP5 MAP2K1 MAP3K1 MAPRE2 MAX MBTPS2 MC1R MDH2 MDM2 MEN1 MGMT MITF MLH1 MLH3 MNX1 MRE11 MSH2 MSH3 MSH6 MTAP MYO1H NBN NEK9 NF1 NF2 NLRP1 NME1 NOTCH3 NR0B1 NR4A3 NR5A1 NRAS NSD1 NUTM1 OCA2 OFD1 PALB2 PALLD PAX3 PAX6 PAX7 PDE6D PDGFB PDGFRA PDGFRB PHF21A PHOX2B PIK3CA PLCD1 PMS1 PMS2 POLH POT1 POU6F2 PRDM16 PRKAR1A PRLR PTCH1 PTCH2 PTEN PTH1R PTPN11 RAD50 RAD51 RAD51C RAD51D RAF1 RB1 RECQL4 RELA RERE REST RET RNF43 RPS19 RSPO1 RUNX1 SDHA SDHAF2 SDHB SDHC SDHD SEC23B SETBP1 SETD2 SF3B1 SIX6 SKI SLC22A18 SLC37A4 SLC45A2 SMAD4 SOS1 SOX2 SOX9 SPRED1 SQSTM1 SRC SRY SSX1 SSX2 STK11 SUFU TAF15 TBX18 TCTN3 TERF2IP TERT TFAP2A TGFBR2 TMEM127 TMEM216 TP53 TRIM28 TRIM37 TRIP13 TRPV3 TSC1 TSC2 TUBB TYR VAMP7 VHL WRN WT1 WWOX XPA XPC ZFPM2

Diseases (215) :618 64755 135100 201 145 2098 500 1333 145001 524 606719 609265 678 910 278740 617088 220295 278730 278800 83469 562 2762 44890 615107 659 79432 64754 249400 90342 157798 79435 2753 113620 79434 902 278700 2136 744 615109 176920 79665 261584 247806 175100 614327 613707 443167 99880 143 610755 130650 155755 259500 1571 750 612160 180295 267000 305000 610651 612219 321 215300 133700 133701 2791 162900 273300 300244 373 137550 163634 296 79474 626 158320 112250 615225 612237 228550 615108 278750 1359 137608 109 158350 1587 180200 221016 1225 268400 105650 610644 798 269150 268210 232240 175050 167250 175200 143400 151623 277700 278720 135400 2026 52022 2028 228600 873 135290 821 606243 3473 39044 608022 610069 163950 654 194070 1052 257300 652 276152 31112 2754 277170 602398 601200 2849 251510 3019 1832 617107 33001 672 146510 312870 2128 180860 194071 1001 218040 135500 606764 312 276300 1552 480536 647 251260 193520 162210 162200 601321 101000 2591 117550 311200 610832 194072 276280 602501 615554 77301 109400 65285 2024 206900 135300 611431 300813 253250 805 538 191100 613254 256370 194080 220 347 114500 276399 29072 523 150800 135150 268220 2612 213504 841 259770 131100 587 176450 637 2387 892 193300 251636 144 137800 370348 617100 99803 1606 256700 601399 115310 209880 661 2505 2151 613013 156610
 

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