Axonal sensorimotor neuropathy

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Axonal sensorimotor neuropathy (in some patients) [OMIM:Axonal sensorimotor neuropathy (in some patients)]
Sensorimotor axonal neuropathy [OMIM:Sensorimotor axonal neuropathy]
Sensorimotor axonal neuropathy (in some patients) [OMIM:Sensorimotor axonal neuropathy (in some patients)]
Quality:
Cross references:
OMIM: "Axonal sensorimotor neuropathy" [OMIM:Axonal sensorimotor neuropathy]
OMIM: "Axonal sensorimotor neuropathy (in some patients)" [OMIM:Axonal sensorimotor neuropathy (in some patients)]
OMIM: "Sensorimotor axonal neuropathy" [OMIM:Sensorimotor axonal neuropathy]
OMIM: "Sensorimotor axonal neuropathy (in some patients)" [OMIM:Sensorimotor axonal neuropathy (in some patients)]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant Charcot-Marie-Tooth disease type 2P (Orphanet:300319)
Autosomal recessive cerebellar ataxia - saccadic intrusion (Orphanet:95434)
Autosomal recessive spastic paraplegia type 26 (Orphanet:101006)
BROWN-VIALETTO-VAN LAERE SYNDROME 2 (OMIM:614707)
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC (OMIM:613640)
NEUROPATHY, HEREDITARY SENSORY, TYPE ID (OMIM:613708)