Abnormality of the medulla oblongata

Symptom Information:

Symptom ID: HPO:0011441
Synonyms:
Medulla anomaly [Orphanet:42690]
Midbrain/brainstem/pons/medulla anomalies [Orphanet:42690]
Quality:
Cross references:
Orphanet:42690 "Midbrain/brainstem/pons/medulla anomalies" [Orphanet:42690]
Is a (Direct Parents):
Orphanet Structural anomalies of the nervous system
HPO         Abnormality of brainstem morphology
Orphanet Abnormality of brainstem morphology
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 4 / 7739
Resource:

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)