Mild pyramidal signs (variable expression)

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Pyramidal signs, mild [OMIM:Pyramidal signs, mild]
Pyramidal signs, mild (uncommon) [OMIM:Pyramidal signs, mild (uncommon)]
Quality:
Cross references:
OMIM: "Mild pyramidal signs (variable expression)" [OMIM:Mild pyramidal signs (variable expression)]
OMIM: "Pyramidal signs, mild" [OMIM:Pyramidal signs, mild]
OMIM: "Pyramidal signs, mild (uncommon)" [OMIM:Pyramidal signs, mild (uncommon)]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome (Orphanet:363429)
Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency (Orphanet:324262)
Hereditary motor and sensory neuropathy type 5 (Orphanet:64751)
Spinocerebellar ataxia type 20 (Orphanet:101110)