Brainstem atrophy

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Brainstem atrophy" [OMIM:Brainstem atrophy]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive spastic paraplegia type 35 (Orphanet:171629)
Combined oxidative phosphorylation defect type 14 (Orphanet:319519)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5 (OMIM:613477)
Infantile onset spinocerebellar ataxia (Orphanet:1186)
Pontocerebellar hypoplasia type 6 (Orphanet:166073)