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
autoimmune hypothyroidism C562768
childhood onset IBGC C536276
idiopathic, childhood-onset basal ganglia calcification C536276
childhood onset bilateral striopallidodentate calcinosis C536276
congenital, 1 capillary malformations C562760
high-grade neuroendocrine carcinoma of the cervix uteri 16276
bilateral striopallidodentate calcinosis, childhood onset C536276
nonarteriosclerotic, idiopathic, childhood-onset cerebral calcification C536276
high-grade neuroendocrine carcinoma of the uterine cervix 16276
poorly differentiated neuroendocrine carcinoma of the cervix uteri 16276
genetic defect in, 3 thyroid hormonogenesis C562769
capillary malformations, congenital, 1 C562760
inflammatory myofibroblastic lung tumor 6276
lung inflammatory myofibroblastic tumor 6276
cerebral calcification, nonarteriosclerotic, childhood onset, idiopathic C536276