MONDO_merge Find_IDs Find_Terms Annotation
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created at 2021-12-22 03:08:20 UTC
updated at 2021-12-22 07:06:09 UTC
MONDO_bioport_pref_name
183,974 entries
Label
Id
CCSF 7990
CPVT 17990
CSCSC 7990
Kunze-Riehm syndrome 7990
axonal, type 2b1 charcot-marie-tooth disease C537990
neuronal, type 2b1 charcot-marie-tooth disease C537990
multiple benign circumferential skin creases on limbs 7990
type 2b1 charcot-marie-tooth disease C537990
type 2b1 charcot-marie-tooth neuropathy C537990
charcot-marie-tooth disease, axonal, autosomal recessive, b1 C537990
charcot-marie-tooth disease, axonal, type 2b1 C537990
Michelin tire baby syndrome 7990
ventricular tachycardia, catecholaminergic polymorphic 17990
charcot-marie-tooth disease, neuronal, type 2b1 C537990
skin creases, multiple benign ring-shaped, of limbs 7990