Frontotemporal atrophy

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Frontotemporal atrophy" [OMIM:Frontotemporal atrophy]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

Glutaryl-CoA dehydrogenase deficiency (Orphanet:25)
Intellectual disability-seizures-hypotonia-ophthalmologic-skeletal anomalies syndrome (Orphanet:369837)
Malonic aciduria (Orphanet:943)