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DOID:0050539 - Charcot-Marie-Tooth disease type 2
Disease Ontology Definition:A Charcot-Marie-Tooth disease characterized by abnormalities in the axon of the peripheral nerve cell.
Synonyms: hereditary motor and sensory neuropathy Guadalajara neuronal type, hereditary motor and sensory neuropathy Okinawa type, hereditary motor and sensory neuropathy type 2
Xenbase Genes
:
mfn2,
hspb1,
rab7a,
atp1a1,
nefl,
dync1h1,
mpz,
nefh,
lmna,
trim2,
hspb8,
dnajb2,
jph1,
tfg,
gars1,
| MONDO:0018993 - Charcot-Marie-Tooth disease type 2 |
| MIM:118230 - CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE |
| MIM:604484 - NEUROPATHY, HEREDITARY MOTOR AND SENSORY, OKINAWA TYPE; HMSNO |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
Charcot-Marie-Tooth disease (is_a)