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, prader-labhart-willi D011218
syndrome, prader-willi D011218
syndrome, royer D011218
syndrome, willi-prader D011218
willi-prader syndrome D011218
labhart willi syndrome D011218
ichthyosis and follicular atrophoderma with hypotrichosis and hypohidrosis 11218
hypotrichosis-congenital ichthyosis syndrome 11218
ichthyosis-follicular atrophoderma-hypotrichosis syndrome 11218
ichthyosis-follicular atrophoderma-hypotrichosis-hypohidrosis syndrome 11218
ichthyosis, congenital, autosomal recessive 11 11218
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