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All terms in MONDO

Label Id Description
maternal disease-related embryofetopathy MONDO_0016678
obsolete rare tumor of neuroepithelial tissue MONDO_0016679
hereditary spastic paraplegia 54 MONDO_0014018
hereditary persistence of fetal hemoglobin-sickle cell disease syndrome MONDO_0016672
localized junctional epidermolysis bullosa, non-Herlitz type MONDO_0016673
junctional epidermolysis bullosa, non-Herlitz type MONDO_0009180
46,XY partial gonadal dysgenesis MONDO_0016674
46,XY disorder of gonadal development MONDO_0017966
distal arthrogryposis type 10 MONDO_0016675
maternal riboflavin deficiency MONDO_0014013
ariboflavinosis MONDO_0004573
disorder of other vitamins and cofactors metabolism and transport MONDO_0017760
Charcot-Marie-Tooth disease axonal type 2Q MONDO_0014012
autosomal recessive congenital ichthyosis 10 MONDO_0014011
sickle cell-hemoglobin d disease syndrome MONDO_0016670
sickle cell-hemoglobin E disease syndrome MONDO_0016671
autosomal recessive congenital ichthyosis 9 MONDO_0014010
cognitive disorder MONDO_0002039
malignant colon neoplasm MONDO_0021063
intestinal cancer MONDO_0005814