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Herb Integrative Database
Traditional Medicine Data Platform
Diseases

Ganglioneuroblastoma

ganglioneuroblastoma

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Entity Type
Diseases
Relation Groups
2
Relation Preview
16

Basic Information

Grouped by core information, identifiers, and descriptions.

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Core Information

Disease Name
Ganglioneuroblastoma
Standard Disease Name
ganglioneuroblastoma
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
D018305
OMIM ID
MTHU010646
UMLS ID
C0206718
HPO ID
No data

Description and Extensions

Description
NCI2016_CDISC_1602D:A malignant neoplasm characterized by the presence of neuroblastic and ganglion cells and a stroma with Schwannian differentiation.|NCI2016_02D:A neuroblastic tumor characterized by the presence of neuroblastic cells, ganglion cells, and a stroma with Schwannian differentiation constituting more than fifty-percent of the tumor volume. There are two histologic subtypes identified: ganglioneuroblastoma, intermixed and ganglioneuroblastoma, nodular.|MSH2017_2016_08_12:A moderately malignant neoplasm composed of primitive neuroectodermal cells dispersed in myxomatous or fibrous stroma intermixed with mature ganglion cells. It may undergo transformation into a neuroblastoma. It arises from the sympathetic trunk or less frequently from the adrenal medulla, cerebral cortex, and other locations. Cervical ganglioneuroblastomas may be associated with HORNER SYNDROME and the tumor may occasionally secrete vasoactive intestinal peptide, resulting in chronic diarrhea.
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