Optic glioma

Symptom Information:

Symptom ID: HPO:0009734
Synonyms:
Optic glioma [OMIM:Optic glioma]
Optic glioma (19%) [OMIM:Optic glioma (19%)]
Optic gliomas [OMIM:Optic gliomas]
Optic glioma [MedDRA:10073338]
Quality:
Cross references:
OMIM: "Optic glioma" [OMIM:Optic glioma]
OMIM: "Optic glioma (19%)" [OMIM:Optic glioma (19%)]
OMIM: "Optic gliomas" [OMIM:Optic gliomas]
Is a (Direct Parents):
HPO         Glioma
MedDRA Ocular neoplasms malignancy unspecified
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the nervous system(HPO:0000707)
          Neoplasm of the nervous system(HPO:0004375)
             Neoplasm of the central nervous system(HPO:0100006)
                Malignant neoplasm of the central nervous system(HPO:0100836)
                   Glioma(HPO:0009733)
                      Optic glioma(HPO:0009734)
          Abnormality of nervous system morphology(HPO:0012639)
             Morphological abnormality of the central nervous system(HPO:0002011)
                Neoplasm of the central nervous system(HPO:0100006)
                   Malignant neoplasm of the central nervous system(HPO:0100836)
                      Glioma(HPO:0009733)
                         Optic glioma(HPO:0009734)
       Neoplasm(HPO:0002664)
          Neoplasm by anatomical site(HPO:0011793)
             Neoplasm of the nervous system(HPO:0004375)
                Neoplasm of the central nervous system(HPO:0100006)
                   Malignant neoplasm of the central nervous system(HPO:0100836)
                      Glioma(HPO:0009733)
                         Optic glioma(HPO:0009734)
MedDRA:
Neoplasms benign, malignant and unspecified (incl cysts and polyps)(MedDRA:10029104)
    Neoplasm of the eye(HPO:0100012)
       Ocular neoplasms malignancy unspecified(MedDRA:10030053)
          Optic glioma(HPO:0009734)
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

17q11 microdeletion syndrome (Orphanet:97685)
17q11.2 microduplication syndrome (Orphanet:139474)
Neurofibromatosis type 1 due to NF1mutation or intragenic deletion (Orphanet:363700)
TUBEROUS SCLEROSIS 1 (OMIM:191100)
TUBEROUS SCLEROSIS 2 (OMIM:613254)
Tuberous sclerosis (Orphanet:805)
[DEL] NEUROFIBROMATOSIS-NOONAN SYNDROME (OMIM:601321)