Unilateral vestibular Schwannoma

Symptom Information:

Symptom ID: HPO:0009590
Synonyms:
Unilateral vestibular schwannoma [OMIM:Unilateral vestibular schwannoma]
Quality:
Cross references:
OMIM: "Unilateral vestibular schwannoma" [OMIM:Unilateral vestibular schwannoma]
Is a (Direct Parents):
HPO         Vestibular Schwannoma
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Neoplasm(HPO:0002664)
          Neoplasm by anatomical site(HPO:0011793)
             Neoplasm of the nervous system(HPO:0004375)
                Neoplasm of the peripheral nervous system(HPO:0100007)
                   Schwannoma(HPO:0100008)
                      Vestibular Schwannoma(HPO:0009588)
                         Unilateral vestibular Schwannoma(HPO:0009590)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system morphology(HPO:0012639)
             Abnormal peripheral nervous system morphology(HPO:0000759)
                Neoplasm of the peripheral nervous system(HPO:0100007)
                   Schwannoma(HPO:0100008)
                      Vestibular Schwannoma(HPO:0009588)
                         Unilateral vestibular Schwannoma(HPO:0009590)
             Morphological abnormality of the central nervous system(HPO:0002011)
                Abnormality of the cranial nerves(HPO:0001291)
                   Abnormality of the vestibulocochlear nerve(HPO:0009591)
                      Vestibular Schwannoma(HPO:0009588)
                         Unilateral vestibular Schwannoma(HPO:0009590)
          Neoplasm of the nervous system(HPO:0004375)
             Neoplasm of the peripheral nervous system(HPO:0100007)
                Schwannoma(HPO:0100008)
                   Vestibular Schwannoma(HPO:0009588)
                      Unilateral vestibular Schwannoma(HPO:0009590)
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

NEUROENDOCRINE CARCINOMA OF SALIVARY GLANDS, SENSORINEURAL HEARINGLOSS, AND ENAMEL HYPOPLASIA (OMIM:603641)
Neurofibromatosis type 2 (Orphanet:637)