-
Neuropathy, hereditary motor and sensory, type 6A
Neuropathy, hereditary motor and sensory, type 6A
MedGen
-
CN305336[conceptid] (1)
MedGen
-
Multiple symmetric lipomatosis
Multiple symmetric lipomatosis
MedGen
-
C0023804[conceptid] (1)
MedGen
-
Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2a2b;
Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2a2b;
MedGen
Your browsing activity is empty.
Activity recording is turned off.
Turn recording back on
See more...