togoid_mondo_label_20251126 Find_IDs Find_Terms Annotation
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created at 2025-11-26 04:53:50 UTC
updated at 2025-11-27 01:00:35 UTC
Mondo ID - Mondo Label
30,114 entries
Label
Id
IgA nephropathy, susceptibility to, 1 0008072
amyotrophic neuralgia 0008076
neuropathy, with paraprotein in serum, cerebrospinal fluid and urine 0008088
osteochondrodysplasia, rhizomelic, with callosal agenesis, thrombocytopenia, hydrocephalus, and hypertension 0008169
hypertrophic osteoarthropathy, primary, autosomal dominant 0008172
Paget disease of bone 3 0008176
Paramolar tubercle of bolk 0008194
Parotidomegaly, hereditary bilateral 0008202
Passovoy factor defect 0008203
Pechet factor deficiency 0008212
Pick disease 0008243
thrombophilia due to protein C deficiency, autosomal dominant 0008316
Pseudoatrophoderma colli 0008325
scapuloperoneal spinal muscular atrophy, autosomal dominant 0008408
Somatomedin, embryonic 0008435