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
brachial amelia, forebrain defects, and facial clefts C536713
iranian variant form mucolipidosis III C565367
epileptic encephalopathy, early infantile, 58 33367
epileptic encephalopathy, early infantile, 58; EIEE58 http://purl.obolibrary.org/obo/MONDO_0033367
multiple, with early-onset diabetes mellitus epiphyseal dysplasia C536739
febrile seizures, familial, 1 7367
febrile seizures, familial, 1; FEB1 http://purl.obolibrary.org/obo/MONDO_0007367
convulsions, familial febrile 7367
convulsions, familial febrile, 1 7367
X-linked, with gynecomastia and obesity mental retardation C536708
congenital woolly hair C536745
encephalopathy, fatal infantile, with olivopontocerebellar hypoplasia C536716
KHDC3L complete hydatidiform mole 13671
winter harding hyde syndrome C536712
anemia, sex-linked hypochromic sideroblastic C536761