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
syndrome, labhart-willi-prader-fanconi D011218
syndrome, prader-labhart-willi D011218
syndrome, prader-willi D011218
syndrome, royer D011218
syndrome, willi-prader D011218
willi-prader syndrome D011218
ichthyosis, congenital, autosomal recessive 11; ARCI11 http://purl.obolibrary.org/obo/MONDO_0011218
ichthyosis, congenital, autosomal recessive type 11 11218
autosomal recessive congenital ichthyosis 11 11218
autosomal recessive congenital ichthyosis type 11 11218
prader labhart willi syndrome D011218
ichthyosis and follicular atrophoderma with hypotrichosis and hypohidrosis 11218
ichthyosis with hypotrichosis, autosomal recessive 11218
autosomal recessive ichthyosis with hypotrichosis 11218
labhart willi syndrome D011218