Human Phenotype Ontology 
Grandparent Node:
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Abnormality of nervous system morphology (HP:0012639)help
Grandparent Node:
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Neoplasm by anatomical site (HP:0011793)help
Parent Node:
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Morphological abnormality of the central nervous system (HP:0002011)help
Parent Node:
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Neoplasm of the nervous system (HP:0004375)help
..Starting node
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Neoplasm of the central nervous system (HP:0100006)help
Term ID: 100006
Name: Neoplasm of the central nervous system
Synonym: Neoplasia of the central nervous system; Neoplasm of the CNS; Tumors of the central nervous system
Definition: A neoplasm of the central nervous system.
Comments:
Reference: HP:0100006
Genes and Diseases:
 
       Child Nodes:
........expandSpinal cord tumor (HP:0010302) help
................... HP:0009713 Spinal hemangioblastoma
........expandNeuronal/glioneuronal neoplasm of the central nervous system (HP:0025170) help
................... HP:0025171 Rosette-forming glioneuronal tumor
........expandBrain neoplasm (HP:0030692) help
................... HP:0030693 Supratentorial neoplasm
........expandBenign neoplasm of the central nervous system (HP:0100835) help
................... HP:0002858 Meningioma
................... HP:0009731 Cerebral hamartomata
................... HP:0010797 Hemangioblastoma
................... HP:0100251 Lipomas of the central neryous system
................... HP:0100312 Cerebral germinoma
................... HP:0200022 Choroid plexus papilloma
........expandMalignant neoplasm of the central nervous system (HP:0100836) help
................... HP:0002885 Medulloblastoma
................... HP:0004376 Neuroblastic tumors
................... HP:0009733 Glioma
................... HP:0030392 Choroid plexus carcinoma
................... HP:0100312 Cerebral germinoma

 Sister Nodes: 
..expandNeoplasm of the peripheral nervous system (HP:0100007) 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:0100006HP:0100006Neoplasm of the central nervous system0EWSR1 CL E G H213083469ORPHA083508133450
HP:0100006HP:0100006Neoplasm of the central nervous system0WT1 CL E G H749083469ORPHA018412796607102
HP:0100006HP:0100006Neoplasm of the central nervous system1EWSR1 CL E G H213083469ORPHA083508133450
HP:0100006HP:0100006Neoplasm of the central nervous system1WT1 CL E G H749083469ORPHA018412796607102
HP:0100006HP:0100006Neoplasm of the central nervous system2EWSR1 CL E G H213083469ORPHA083508133450
HP:0100006HP:0100006Neoplasm of the central nervous system2WT1 CL E G H749083469ORPHA018412796607102
HP:0100006HP:0100006Neoplasm of the central nervous system3EWSR1 CL E G H213083469ORPHA083508133450
HP:0100006HP:0100006Neoplasm of the central nervous system3WT1 CL E G H749083469ORPHA018412796607102
HP:0100006HP:0100006Neoplasm of the central nervous system4EWSR1 CL E G H213083469ORPHA083508133450
HP:0100006HP:0100006Neoplasm of the central nervous system4WT1 CL E G H749083469ORPHA018412796607102
HP:0100006HP:0100006Neoplasm of the central nervous system5EWSR1 CL E G H213083469ORPHA083508133450
HP:0100006HP:0100006Neoplasm of the central nervous system5WT1 CL E G H749083469ORPHA018412796607102


Genes (113) :ADAMTS3 AKT1 ALX1 ALX3 APC ARMC5 ASCL1 BAP1 BDNF BRAF BRD4 C11ORF95 CCBE1 CCM2 CDKN2A CHEK2 CPLANE1 CTNNB1 DICER1 EDN3 EPCAM ERBB2 EWSR1 FAN1 FAT4 FGFR1 FH FLI1 GABRD GDNF GLI3 GNAS GPC3 GPC4 IDH1 IDH2 KCNAB2 KEAP1 KIAA0753 KIF1B KIF7 KLLN KRAS KRIT1 LMNA LRP5 MAPRE2 MAX MDH2 MLH1 MLH3 MN1 MSH2 MSH3 MSH6 MYO1H NBN NF1 NF2 NME1 NOTCH3 NRAS NTHL1 NUTM1 OCRL OFD1 PALB2 PDCD10 PDE6D PDGFB PDGFRB PHOX2B PIK3CA PMS1 PMS2 POLD1 POLE PRDM16 PTCH1 PTCH2 PTEN PTPN11 RAF1 RB1 RELA RERE RET RUNX1 SDHA SDHAF2 SDHB SDHC SDHD SEC23B SETBP1 SIX6 SKI SMARCB1 SOX2 SUFU TCTN3 TGFBR2 TMEM127 TMEM216 TP53 TSC1 TSC2 TUBB VHL WDPCP WRN WT1 ZSWIM6

Diseases (87) :83469 2136 79665 251636 144 370348 162210 162091 2591 534 447877 99966 1338 201 744 615109 247806 175100 189427 614327 221061 609265 155255 601200 613001 79474 259770 276300 607174 647 251260 162200 637 101000 249400 454840 616415 610832 615108 602501 77301 109400 109 158350 609322 2807 193300 902 277700 99803 500 443167 155755 2754 277170 276399 137800 29072 1606 672 146510 373 163634 480536 617100 601321 256700 311200 180200 601399 115310 798 206900 805 191100 613254 892 1827 306542 391474 136760 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.