Insidious onset

Symptom Information:

Symptom ID: HPO:0003587
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
HPO         Speed of onset
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant optic atrophy, classic type (Orphanet:98673)
Autosomal dominant spastic paraplegia type 3 (Orphanet:100984)
Autosomal dominant spastic paraplegia type 4 (Orphanet:100985)
Autosomal dominant spastic paraplegia type 6 (Orphanet:100988)
Autosomal dominant spastic paraplegia type 8 (Orphanet:100989)
Charcot-Marie-Tooth disease type 1A (Orphanet:101081)
Charcot-Marie-Tooth disease type 1B (Orphanet:101082)
Monomelic amyotrophy (Orphanet:65684)
PARKINSON DISEASE 18, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO (OMIM:614251)
PARKINSON DISEASE, LATE-ONSET (OMIM:168600)
Spinocerebellar ataxia type 30 (Orphanet:211017)