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
type ii methemoglobinemia C537841
type ii nadh-cytochrome b5 reductase deficiency C537841
integument hypersensitivity reaction type II disease 17841
congenital, autosomal recessive methemoglobinemia C537841
nadh-cytochrome b5 reductase deficiency C537841
nadh-cytochrome b5 reductase deficiency, type i C537841
nadh-cytochrome b5 reductase deficiency, type ii C537841
small patella syndrome 7841
congenital coxa vara, patella aplasia and tarsal synostosis 7841
autoimmune disease of skin and connective tissue 17841
small patella syndrome; SPS http://purl.obolibrary.org/obo/MONDO_0007841
autoimmune disease with skin involvement 17841