Benign neoplasm of the central nervous system
Symptom Information:
Symptom ID: | HPO:0100835 | ||||||||||||
Synonyms: |
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Is a (Direct Parents): |
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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 central nervous system(HPO:0100006) Benign neoplasm of the central nervous system(HPO:0100835) Abnormality of the nervous system(HPO:0000707) Neoplasm of the nervous system(HPO:0004375) Neoplasm of the central nervous system(HPO:0100006) Benign neoplasm of the central nervous system(HPO:0100835) Abnormality of nervous system morphology(HPO:0012639) Morphological abnormality of the central nervous system(HPO:0002011) Neoplasm of the central nervous system(HPO:0100006) Benign neoplasm of the central nervous system(HPO:0100835) MedDRA: Nervous system disorders(MedDRA:10029205) Benign neoplasm of the central nervous system(HPO:0100835) |
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Database Frequency: | 12 / 7739 | ||||||||||||
Resource: |
All diseases associated with this symptom:
Alveolar echinococcosis | (Orphanet:284) |
Distal 7q11.23 microduplication syndrome | (Orphanet:261102) |
Heart defect - tongue hamartoma - polysyndactyly | (Orphanet:1338) |
Hennekam syndrome | (Orphanet:2136) |
Infantile myofibromatosis | (Orphanet:2591) |
Lymphedema - distichiasis | (Orphanet:33001) |
Multiple endocrine neoplasia type 2 | (Orphanet:653) |
Neurofibromatosis type 1 | (Orphanet:636) |
Neurofibromatosis type 2 | (Orphanet:637) |
Non-polyposis Turcot syndrome | (Orphanet:99817) |
Oculocerebrorenal syndrome | (Orphanet:534) |
Pai syndrome | (Orphanet:1993) |