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encyclopedia of Rare Disease Annotation for Precision Medicine

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	hemangiopericytoma

Disease ID	1208
Disease	hemangiopericytoma
Definition	A tumor composed of spindle cells with a rich vascular network, which apparently arises from pericytes, cells of smooth muscle origin that lie around small vessels. Benign and malignant hemangiopericytomas exist, and the rarity of these lesions has led to considerable confusion in distinguishing between benign and malignant variants. (From Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1364)
Synonym	[m]haemangiopericytoma nos haemangiopericytic meningioma [obs] haemangiopericytoma haemangiopericytoma, nos hemangiopericytic meningioma [obs] hemangiopericytoma (disorder) hemangiopericytoma (morphologic abnormality) hemangiopericytoma [disease/finding] hemangiopericytoma, nos hemangiopericytomas hpa - haemangiopericytoma hpa - hemangiopericytoma perithelioma
DOID	DOID:264
UMLS	C0018922
MeSH	D006393
SNOMED-CT	SNOMEDCT_US_2016_09_01:134335004
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:13) C0153676 \| lung metastases \| 2 C0008487 \| chordoma \| 1 C0003857 \| arteriovenous malformation \| 1 C1334801 \| monophasic synovial sarcoma \| 1 C0039101 \| synovial sarcoma \| 1 C0025286 \| meningioma \| 1 C0494165 \| hepatic metastases \| 1 C0020598 \| hypoglycemia \| 1 C1261473 \| sarcoma \| 1 C0020538 \| hypertension \| 1 C0008479 \| chondrosarcomas \| 1 C1527311 \| brain edema \| 1 C1266119 \| solitary fibrous tumor \| 1
Curated Gene	Entrez_id \| Symbol \| Resource(Total Genes:2) 6778 \| STAT6 \| ORPHANET 4665 \| NAB2 \| ORPHANET
Inferring Gene	(Waiting for update.)
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:48) 54880 \| BCOR \| 1.204 \| DISEASES 55814 \| BDP1 \| 2.211 \| DISEASES 800 \| CALD1 \| 4.336 \| DISEASES 4267 \| CD99 \| 2.349 \| DISEASES 64764 \| CREB3L2 \| 3.471 \| DISEASES 29119 \| CTNNA3 \| 1.647 \| DISEASES 1499 \| CTNNB1 \| 1.815 \| DISEASES 192668 \| CYS1 \| 1.659 \| DISEASES 1649 \| DDIT3 \| 1.159 \| DISEASES 1809 \| DPYSL3 \| 1.772 \| DISEASES 10938 \| EHD1 \| 1.132 \| DISEASES 2050 \| EPHB4 \| 1.214 \| DISEASES 2120 \| ETV6 \| 1.924 \| DISEASES 2157 \| F8 \| 1.135 \| DISEASES 2197 \| FAU \| 2.079 \| DISEASES 388698 \| FLG2 \| 2.798 \| DISEASES 26061 \| HACL1 \| 3.576 \| DISEASES 3039 \| HBA1 \| 3.956 \| DISEASES 3481 \| IGF2 \| 3.358 \| DISEASES 55683 \| KANSL3 \| 2.116 \| DISEASES 22944 \| KIN \| 2.141 \| DISEASES 3855 \| KRT7 \| 1.191 \| DISEASES 4151 \| MB \| 1.371 \| DISEASES 4193 \| MDM2 \| 1.29 \| DISEASES 56955 \| MEPE \| 1.491 \| DISEASES 2315 \| MLANA \| 1.114 \| DISEASES 4311 \| MME \| 1.285 \| DISEASES 4782 \| NFIC \| 1.193 \| DISEASES 4916 \| NTRK3 \| 1.659 \| DISEASES 7849 \| PAX8 \| 1.357 \| DISEASES 728378 \| POTEF \| 1.288 \| DISEASES 83695 \| RHNO1 \| 1.275 \| DISEASES 6234 \| RPS28 \| 2.834 \| DISEASES 6424 \| SFRP4 \| 1.299 \| DISEASES 6525 \| SMTN \| 1.785 \| DISEASES 23583 \| SMUG1 \| 1.736 \| DISEASES 6760 \| SS18 \| 2.965 \| DISEASES 6756 \| SSX1 \| 1.116 \| DISEASES 727837 \| SSX2B \| 2.564 \| DISEASES 51684 \| SUFU \| 1.241 \| DISEASES 7033 \| TFF3 \| 1.787 \| DISEASES 7088 \| TLE1 \| 2.433 \| DISEASES 7155 \| TOP2B \| 1.066 \| DISEASES 7170 \| TPM3 \| 1.251 \| DISEASES 7171 \| TPM4 \| 1.968 \| DISEASES 7321 \| UBE2D1 \| 5.01 \| DISEASES 7422 \| VEGFA \| 1.587 \| DISEASES 81030 \| ZBP1 \| 1.718 \| DISEASES
Locus	(Waiting for update.)

Disease ID	1208
Disease	hemangiopericytoma
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:12) HP:0002664 \| Neoplasia \| 9 HP:0012570 \| Synovial sarcoma \| 1 HP:0002170 \| Intracranial hemorrhage \| 1 HP:0012721 \| Venous malformations \| 1 HP:0002858 \| Mengiomia \| 1 HP:0100026 \| Arteriovenous malformation \| 1 HP:0001943 \| Hypoglycemia \| 1 HP:0010762 \| Chordoma \| 1 HP:0000822 \| Hypertension \| 1 HP:0100242 \| Sarcoma \| 1 HP:0000969 \| Dropsy \| 1 HP:0002181 \| Cerebral edema \| 1

Disease ID	1208
Disease	hemangiopericytoma
Manually Symptom	UMLS \| Name(Total Manually Symptoms:7) C1963215 \| pneumothorax C1527197 \| angioblastic meningioma C1274103 \| oncogenic osteomalacia C0494165 \| hepatic metastasis C0494165 \| hepatic metastases C0153687 \| cutaneous metastasis C0029166 \| oral manifestations
Text Mined Symptom	UMLS \| Name \| Sentences' Count(Total Symptoms:1) C0494165 \| hepatic metastases \| 1

Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)

Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)

All Snps(Total Genotypes:0)
(Waiting for update.)

GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)

GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)

Mapped by lexical matching(Total Items:0)
(Waiting for update.)

Mapped by homologous gene(Total Items:0)
(Waiting for update.)

Disease ID	1208
Disease	hemangiopericytoma
Case	(Waiting for update.)

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