PedAM

Pediatric Disease Annotations & Medicines


	central neurocytoma

Disease ID	918
Disease	central neurocytoma
Definition	An intraventricular neuronal neoplasm composed of uniform round cells with neuronal differentiation. It is typically located in the lateral ventricles in the region of the foramen of Monro. It generally affects young adults and has a favorable prognosis. (Adapted from WHO)
Synonym	central neurocytoma (morphologic abnormality) central neurocytoma (who grade ii) central neurocytoma - histology central neurocytoma - histology (morphologic abnormality) central neurocytomas lipomatous medulloblastoma medullocytoma neurocytoma, central neurocytomas, central neurolipocytoma
Orphanet	ORPHANET:73256
DOID	DOID:14174 DOID:6458
UMLS	C0206719
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:2) C0205945 \| spindle cell sarcoma \| 1 C0028945 \| oligodendroglioma \| 1
Curated Gene	(Waiting for update.)
Inferring Gene	(Waiting for update.)
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:33) 2026 \| ENO2 \| DISEASES 1611 \| DAP \| DISEASES 51185 \| CRBN \| DISEASES 2670 \| GFAP \| DISEASES 2660 \| MSTN \| DISEASES 3417 \| IDH1 \| DISEASES 6855 \| SYP \| DISEASES 7157 \| TP53 \| DISEASES 4613 \| MYCN \| DISEASES 3081 \| HGD \| DISEASES 9510 \| ADAMTS1 \| DISEASES 6853 \| SYN1 \| DISEASES 5346 \| PLIN1 \| DISEASES 274 \| BIN1 \| DISEASES 10397 \| NDRG1 \| DISEASES 127066 \| OR14C36 \| DISEASES 55553 \| SOX6 \| DISEASES 10215 \| OLIG2 \| DISEASES 23583 \| SMUG1 \| DISEASES 23136 \| EPB41L3 \| DISEASES 5725 \| PTBP1 \| DISEASES 4745 \| NELL1 \| DISEASES 4133 \| MAP2 \| DISEASES 10763 \| NES \| DISEASES 5728 \| PTEN \| DISEASES 160897 \| GPR180 \| DISEASES 116448 \| OLIG1 \| DISEASES 80310 \| PDGFD \| DISEASES 6295 \| SAG \| DISEASES 9048 \| ARTN \| DISEASES 146713 \| RBFOX3 \| DISEASES 4753 \| NELL2 \| DISEASES 10381 \| TUBB3 \| DISEASES
Locus	(Waiting for update.)

Disease ID	918
Disease	central neurocytoma
Integrated Phenotype	HPO \| Name(Total Integrated Phenotypes:13) HP:0001251 \| Ataxia HP:0002516 \| Increased intracranial pressure HP:0002514 \| Cerebral calcification HP:0001254 \| Lethargy HP:0003487 \| Babinski sign HP:0002315 \| Headache HP:0000360 \| Tinnitus HP:0007021 \| Pain insensitivity HP:0000238 \| Hydrocephalus HP:0002017 \| Nausea and vomiting HP:0003401 \| Paresthesia HP:0010576 \| Intracranial cystic lesion HP:0001259 \| Coma
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:3) HP:0000718 \| Aggressive behaviour \| 1 HP:0000969 \| Dropsy \| 1 HP:0002888 \| Ependymoma \| 1

Disease ID	918
Disease	central neurocytoma
Manually Symptom	UMLS \| Name(Total Manually Symptoms:1) C0019080 \| hemorrhage
Text Mined Symptom	UMLS \| Name \| Sentences' Count(Total Symptoms:1) C0019080 \| hemorrhage \| 1

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.)

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