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
muscular dystrophy, congenital, Pomt1-Related http://purl.obolibrary.org/obo/MONDO_0013159
muscular dystrophy, congenital, Pomt1-related 13159
fetal ovarian cyst 43154
neonatal ovarian cyst 43154
familial multilocular cystic disease of the jaws 7315
Hageman Factor deficiency 9315
factor 12 deficiency 9315
factor XII deficiency 9315
factor XII deficiency disease 9315
iduronate 2-sulfatase deficiency type A 16315
chromosome 10q deletion 12315
chromosome 10q26 deletion syndrome 12315
distal 10q deletion syndrome 12315
insulin-dependent, 18 diabetes mellitus C565315
craniosynostosis 7, digenic 44315