Skip to main content
Diseases

Aase Syndrome

aase syndrome

Entity Type
Diseases
Relation Groups
1
Relation Preview
8

Basic Information

Grouped by core information, identifiers, and descriptions.

Quick relations do not expand inferred candidates by default. Load path-derived ingredients or herbs when needed.

Core Information

Disease Name
Aase Syndrome
Standard Disease Name
aase syndrome
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
No data
OMIM ID
No data
UMLS ID
C1708954
HPO ID
No data

Description and Extensions

Description
NCI2016_02D:A rare extragonadal germ cell tumor that arises from the mediastinum and is associated with the presence of a somatic-type malignant component. The somatic malignancy is usually a sarcoma (e.g., embryonal rhabdomyosarcoma, angiosarcoma, or leiomyosarcoma), adenocarcinoma, squamous cell carcinoma, adenosquamous carcinoma, or primitive neuroectodermal tumor. The prognosis is poor.
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
03
FLI1
Fli-1 proto-oncogene, ETS transcription factor
Fli-1 proto-oncogene, ETS transcription factor
06
KCNN4
potassium calcium-activated channel subfamily N member 4
potassium calcium-activated channel subfamily N member 4