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
autosomal recessive 1b deafness C567213
autosomal dominant 4 mental retardation C567240
1.35-mb chromosome 1q21.1 deletion syndrome C567291
kallmann syndrome 5 C567220
autosomal dominant 2b deafness C567214
diamond-blackfan anemia 5 C567280
autosomal dominant 5 mental retardation C567234
infantile hypertrophic, 5 pyloric stenosis C567283
autosomal dominant 59 deafness C567216
diamond-blackfan anemia 7 C567254
infection by Blastomyces dermatitidis 5672
retinitis pigmentosa 7 with bull's-eye maculopathy C567264
diamond-blackfan anemia 8 C567253
autosomal dominant 3 mental retardation C567241
hearing loss, ataxia, retinitis pigmentosa, and cataract polyneuropathy C567203