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

There is 0 pattern entry.

Label
Id
PHA2E 13782
duplication 7q C537821
8p- syndrome (partial) C537826
partial deletion (short arm) chromosome 8 C537826
deletion 8p23 1 C537827
monosomy 8p23 1 C537827
monosomy 8p23 1 chromosome 8 C537827
pseudohypoaldosteronism type 2 caused by mutation in CUL3 13782
pseudohypoaldosteronism type 2 caused by mutation in Cul3 13782
pseudohypoaldosteronism type 2E 13782
pseudohypoaldosteronism, type 2E 13782
partial monosomy 8p2 chromosome 8 C537826
pseudohypoaldosteronism, type IIE 13782
pseudohypoaldosteronism, type IIE; PHA2E http://purl.obolibrary.org/obo/MONDO_0013782
macrophagic myofasciitis, childhood C537829
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