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
radiosensitivity, immunodeficiency, dysmorphic features, and learning difficulties 12764
multicystic renal dysplasia, bilateral 27676
Hemorrhagiparous thrombocytic dystrophy 9276
congenital muscular dystrophy due to dystroglycanopathy 18276
epileptic encephalopathy, early infantile, 76 32768
autosomal recessive early-onset parkinson disease 6 C565276
autosomal recessive early-onset, digenic, pink1-dj1 parkinson disease C565276
gall bladder empyema D002764
urinary bladder epidermoid carcinoma 2760
developmental and epileptic encephalopathy, 76 32768
glandular cell epithelial neoplasm 24276
glandular cell epithelium neoplasm 24276
dental caries extending into pulp 5276
idiopathic basal ganglia calcification, childhood onset C536276
epilepsy, idiopathic generalized, susceptibility to, 5 12760