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
postaxial polydactyly, and hypospadias autosomal dominant preaxial deficiency C538278
carcinoma, neuroendocrine D018278
carcinomas, neuroendocrine D018278
neuroendocrine carcinomas D018278
postaxial polydactyly and hypospadias preaxial deficiency C538278
postaxial polydactyly, and hypospadias preaxial deficiency C538278
congenital muscular dystrophy with intellectual disability 18278
CMD 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