JSON

All terms in MONDO

Label Id Description
SAPHO syndrome MONDO_0019266
infantile neuronal ceroid lipofuscinosis MONDO_0019261
autosomal erythropoietic protoporphyria MONDO_0019263
cataract 13 with adult I phenotype MONDO_0007289
obsolete unclassified primitive or secondary maculopathy MONDO_0020244
obsolete colobomatous and areolar dystrophy MONDO_0020243
cataract 41 MONDO_0007287
cataract 6 multiple types MONDO_0007288
obsolete unclassified familial retinal dystrophy MONDO_0020241
cataract 1 multiple types MONDO_0007285
cataract 30 MONDO_0007286
growth hormone secreting pituitary adenoma 1 MONDO_0007052
non-syndromic complex polydactyly MONDO_0034671
restless legs syndrome, susceptibility to, 1 MONDO_0007053
non-syndromic postaxial polydactyly MONDO_0034670
acromegaloid changes, cutis verticis gyrata, and corneal leukoma MONDO_0007050
acromegaloid facial appearance syndrome MONDO_0007051
obsolete rare genetic cardiac disease MONDO_0020029
obsolete rare allergic respiratory disease MONDO_0020028
obsolete rare maxillo-facial surgical disease MONDO_0019038