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
CMD-MR 18278
JPHT 8278
jPS/Hht 8278
JP/Hht syndrome 8278
guttmacher syndrome C538278
CMD with intellectual disability 18278
carcinoma, neuroendocrine D018278
carcinomas, neuroendocrine D018278
neuroendocrine carcinomas D018278
congenital muscular dystrophy with intellectual disability 18278
juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome 8278
juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome; JPHT http://purl.obolibrary.org/obo/MONDO_0008278
telangiectasia, hereditary hemorrhagic, with juvenile polyposis coli 8278
postaxial polydactyly, and hypospadias autosomal dominant preaxial deficiency C538278
postaxial polydactyly and hypospadias preaxial deficiency C538278