Abnormality of the medulla oblongata
Symptom Information:
Symptom ID: | HPO:0011441 | ||||||
Synonyms: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
MedDRA: |
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Database Frequency: | 4 / 7739 | ||||||
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All diseases associated with this symptom:
CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED | (OMIM:302900) |
Combined oxidative phosphorylation defect type 15 | (Orphanet:319524) |
FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA | (OMIM:229310) |
Friedreich ataxia 2 | (OMIM:601992) |