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
POMT2 autosomal recessive limb-girdle muscular dystrophy 13162
autosomal recessive spastic paraplegia type 65 13165
dilated cardiomyopathy type 1DD 13168
autosomal recessive spastic paraplegia 45 13165
5p13 microduplication syndrome 13169
gamma aminobutyrate transaminase deficiency 13166
gamma-aminobutyric acid transaminase deficiency 13166
cardiomyopathy, dilated, type 1Dd 13168
nephronophthisis-like nephropathy type 1 13163