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
duplication 7p C537819
aarau disease C563781
reticular erythrokeratoderma C563781
pseudohypoaldosteronism type 2 caused by mutation in KLHL3 13781
pseudohypoaldosteronism type 2D 13781
pseudohypoaldosteronism, type 2D 13781
partial trisomy 6q chromosome 6 C537810
partial trisomy 6q syndrome C537810
monosomy chromosome 7 C537814
ring chromosome 7 syndrome C537813
partial monosomy 7p chromosome 7 C537818
pseudohypoaldosteronism, type IID 13781
pseudohypoaldosteronism, type IID; PHA2D http://purl.obolibrary.org/obo/MONDO_0013781
acute bronchitis and bronchiolitis 3781
recurrent wheezy bronchitis 3781