Normal or mildly decreased motor nerve conduction velocities (NCV)

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Normal or mildly decreased motor nerve conduction velocity (NCV) [OMIM:Normal or mildly decreased motor nerve conduction velocity (NCV)]
Normal or mildly decreased motor nerve conduction velocity (NCV) (greater than 38 m/s) [OMIM:Normal or mildly decreased motor nerve conduction velocity (NCV) (greater than 38 m/s)]
Quality:
Cross references:
OMIM: "Normal or mildly decreased motor nerve conduction velocities (NCV)" [OMIM:Normal or mildly decreased motor nerve conduction velocities (NCV)]
OMIM: "Normal or mildly decreased motor nerve conduction velocity (NCV)" [OMIM:Normal or mildly decreased motor nerve conduction velocity (NCV)]
OMIM: "Normal or mildly decreased motor nerve conduction velocity (NCV) (greater than 38 m/s)" [OMIM:Normal or mildly decreased motor nerve conduction velocity (NCV) (greater than 38 m/s)]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 15 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant Charcot-Marie-Tooth disease type 2A1 (Orphanet:99946)
Autosomal dominant Charcot-Marie-Tooth disease type 2A2 (Orphanet:99947)
Autosomal dominant Charcot-Marie-Tooth disease type 2B (Orphanet:99936)
Autosomal dominant Charcot-Marie-Tooth disease type 2E (Orphanet:99939)
Autosomal dominant Charcot-Marie-Tooth disease type 2F (Orphanet:99940)
Autosomal dominant Charcot-Marie-Tooth disease type 2G (Orphanet:99941)
Autosomal dominant Charcot-Marie-Tooth disease type 2N (Orphanet:228174)
Autosomal dominant Charcot-Marie-Tooth disease type 2O (Orphanet:284232)
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE (OMIM:607706)
Charcot-Marie-Tooth disease type 2B1 (Orphanet:98856)
Charcot-Marie-Tooth disease type 2B2 (Orphanet:101101)
GIANT AXONAL NEUROPATHY 2, AUTOSOMAL DOMINANT (OMIM:610100)
Hereditary motor and sensory neuropathy type 5 (Orphanet:64751)
Hereditary motor and sensory neuropathy type 6 (Orphanet:90120)
Hereditary sensory and autonomic neuropathy with spastic paraplegia (Orphanet:139578)