PedAM

Pediatric Disease Annotations & Medicines


	choroid plexus papilloma

Disease ID	580
Disease	choroid plexus papilloma
Definition	A usually benign neoplasm that arises from the cuboidal epithelium of the choroid plexus and takes the form of an enlarged CHOROID PLEXUS, which may be associated with oversecretion of CSF. The tumor usually presents in the first decade of life with signs of increased intracranial pressure including HEADACHES; ATAXIA; DIPLOPIA; and alterations of mental status. In children it is most common in the lateral ventricles and in adults it tends to arise in the fourth ventricle. Malignant transformation to choroid plexus carcinomas may rarely occur. (Adams et al., Principles of Neurology, 6th ed, p667; DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2072)
Synonym	[m]choroid plexus papilloma nos [m]choroid plexus papilloma nos (morphologic abnormality) brain tumor, choroid plexus papilloma choroid plexus papilloma (morphologic abnormality) choroid plexus papilloma, no icd-o subtype choroid plexus papilloma, no icd-o subtype (morphologic abnormality) choroid plexus papilloma, no international classification of diseases for oncology subtype choroid plexus papilloma, no international classification of diseases for oncology subtype (morphologic abnormality) choroid plexus papilloma, nos choroid plexus papillomas choroid plexus, papilloma intracranial neoplasm, choroid plexus papilloma papilloma of choroid plexus papilloma of the choroid plexus papilloma, choroid plexus papilloma, choroid plexus [disease/finding] papilloma, choroid plexus, benign papillomas, choroid plexus
Orphanet	ORPHANET:2807
OMIM	OMIM:260500
DOID	DOID:2626
UMLS	C0205770
MeSH	D020288
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:1) C1318558 \| congenital melanocytic nevus \| 1
Curated Gene	Entrez_id \| Symbol \| Resource(Total Genes:1) TP53 \| 7157 \| CLINVAR;CTD_human;ORPHANET
Inferring Gene	(Waiting for update.)
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:66) 84245 \| MRI1 \| DISEASES 1048 \| CEACAM5 \| DISEASES 2026 \| ENO2 \| DISEASES 51364 \| ZMYND10 \| DISEASES 3485 \| IGFBP2 \| DISEASES 3769 \| KCNJ13 \| DISEASES 7276 \| TTR \| DISEASES 7291 \| TWIST1 \| DISEASES 9513 \| FXR2 \| DISEASES 3852 \| KRT5 \| DISEASES 2670 \| GFAP \| DISEASES 759 \| CA1 \| DISEASES 301 \| ANXA1 \| DISEASES 4001 \| LMNB1 \| DISEASES 999 \| CDH1 \| DISEASES 9368 \| SLC9A3R1 \| DISEASES 6598 \| SMARCB1 \| DISEASES 6855 \| SYP \| DISEASES 4854 \| NOTCH3 \| DISEASES 10000 \| AKT3 \| DISEASES 4060 \| LUM \| DISEASES 7157 \| TP53 \| DISEASES 3358 \| HTR2C \| DISEASES 1030 \| CDKN2B \| DISEASES 11197 \| WIF1 \| DISEASES 6781 \| STC1 \| DISEASES 6271 \| S100A1 \| DISEASES 3856 \| KRT8 \| DISEASES 246 \| ALOX15 \| DISEASES 2921 \| CXCL3 \| DISEASES 7373 \| COL14A1 \| DISEASES 5055 \| SERPINB2 \| DISEASES 27043 \| PELP1 \| DISEASES 121340 \| SP7 \| DISEASES 6373 \| CXCL11 \| DISEASES 8793 \| TNFRSF10D \| DISEASES 8837 \| CFLAR \| DISEASES 55 \| ACPP \| DISEASES 3855 \| KRT7 \| DISEASES 2192 \| FBLN1 \| DISEASES 5915 \| RARB \| DISEASES 124976 \| SPNS2 \| DISEASES 5357 \| PLS1 \| DISEASES 3572 \| IL6ST \| DISEASES 2272 \| FHIT \| DISEASES 9962 \| SLC23A2 \| DISEASES 8794 \| TNFRSF10C \| DISEASES 11186 \| RASSF1 \| DISEASES 1612 \| DAPK1 \| DISEASES 6364 \| CCL20 \| DISEASES 6663 \| SOX10 \| DISEASES 2153 \| F5 \| DISEASES 10763 \| NES \| DISEASES 80036 \| TRPM3 \| DISEASES 55966 \| AJAP1 \| DISEASES 10514 \| MYBBP1A \| DISEASES 2878 \| GPX3 \| DISEASES 3875 \| KRT18 \| DISEASES 342527 \| SMTNL2 \| DISEASES 825 \| CAPN3 \| DISEASES 6295 \| SAG \| DISEASES 3481 \| IGF2 \| DISEASES 22862 \| FNDC3A \| DISEASES 9774 \| BCLAF1 \| DISEASES 6207 \| RPS13 \| DISEASES 124975 \| GGT6 \| DISEASES
Locus	(Waiting for update.)

Disease ID	580
Disease	choroid plexus papilloma
Integrated Phenotype	HPO \| Name(Total Integrated Phenotypes:7) HP:0001085 \| Papilledema HP:0000238 \| Nonsyndromal hydrocephalus HP:0002315 \| Headaches HP:0001250 \| Seizures HP:0200022 \| Choroid plexus papilloma HP:0002018 \| Nausea HP:0002013 \| Emesis
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:6) HP:0002664 \| Neoplasia \| 2 HP:0002888 \| Ependymoma \| 1 HP:0001618 \| Dysphonia \| 1 HP:0003764 \| Naevus \| 1 HP:0010819 \| drop attacks \| 1 HP:0000995 \| Beauty mark \| 1

Disease ID	580
Disease	choroid plexus papilloma
Manually Symptom	UMLS \| Name(Total Manually Symptoms:5) C1963137 \| hydrocephalus C0221391 \| melanosis C0158951 \| fetal hemorrhage C0078981 \| arachnoid cyst C0009451 \| communicating hydrocephalus
Text Mined Symptom	(Waiting for update.)

Manually Genotype(Total Text Mining 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.)

Chemical(Total Drugs:0)
(Waiting for update.)

FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)

FDA labeling changes(Total Drugs:0)
(Waiting for update.)

Web
Analytics