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Diseases

Peroxisome Biogenesis Disorder 3B

peroxisome biogenesis disorder 3b

Entity Type
Diseases
Relation Groups
1
Relation Preview
5

Basic Information

Grouped by core information, identifiers, and descriptions.

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Core Information

Disease Name
Peroxisome Biogenesis Disorder 3B
Standard Disease Name
peroxisome biogenesis disorder 3b
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
D005909
OMIM ID
137800|MTHU036792
UMLS ID
C1621958
HPO ID
No data

Description and Extensions

Description
HPO2016_07_04:A tumor arising from glia in the central nervous system with macroscopic regions of necrosis and hemorrhage. Microscopically, glioblastoma multiforme is characterized by regions of pseudopalisading necrosis, pleomorphic nuclei and cells, and microvascular proliferation. [HPO:probinson, pmid:10841526]|CSP2006:malignant form of astrocytoma histologically characterized by pleomorphism of cells, nuclear atypia, microhemorrhage and necrosis; may arise in any region of the central nervous system, with a predilection for the cerebral hemispheres, basal ganglia, and commissural pathways.|CHV2011_02:a type of brain tumor|CHV2011_02:a type of brain tumor
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease5 Targets
01
PEX1
peroxisomal biogenesis factor 1
peroxisomal biogenesis factor 1
03
PEX2
peroxisomal biogenesis factor 2
peroxisomal biogenesis factor 2
05
PEX5
peroxisomal biogenesis factor 5
peroxisomal biogenesis factor 5