Diffuse cerebral atrophy
Symptom Information:
Symptom ID: | HPO:0002506 | |||
Synonyms: |
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HPO:
MedDRA: |
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Database Frequency: | 9 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Biotinidase deficiency | (Orphanet:79241) |
CLN13 disease | (Orphanet:352709) |
Fragile X-associated tremor/ataxia syndrome | (Orphanet:93256) |
GM1 gangliosidosis type 3 | (Orphanet:79257) |
Krabbe disease | (Orphanet:487) |
Leukoencephalopathy - metaphyseal chondrodysplasia | (Orphanet:83629) |
MERRF | (Orphanet:551) |
MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY | (OMIM:613668) |
Spinocerebellar ataxia type 17 | (Orphanet:98759) |