Pyramidal features

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Pyramidal features (rare) [OMIM:Pyramidal features (rare)]
Quality:
Cross references:
OMIM: "Pyramidal features" [OMIM:Pyramidal features]
OMIM: "Pyramidal features (rare)" [OMIM:Pyramidal features (rare)]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant Charcot-Marie-Tooth disease type 2A2 (Orphanet:99947)
Charcot-Marie-Tooth disease type 2H (Orphanet:101102)