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All terms in MONDO

Label Id Description
leukoencephalopathy, hereditary diffuse, with spheroids 2 MONDO_0030634
obsolete extraskeletal mesenchymal chondrosarcoma MONDO_0003043
obsolete extraosseous chondrosarcoma MONDO_0003044
anal gland neoplasm MONDO_0003045
retrograde amnesia MONDO_0003040
pediatric mesenchymal chondrosarcoma MONDO_0003041
adult mesenchymal chondrosarcoma MONDO_0003042
lissencephaly with cerebellar hypoplasia type F MONDO_0015039
lissencephaly with cerebellar hypoplasia type E MONDO_0015038
lissencephaly with cerebellar hypoplasia type D MONDO_0015037
glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form MONDO_0017699
glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form MONDO_0017695
spastic paraplegia 86, autosomal recessive MONDO_0030673
intraneural perineurioma MONDO_0015032
glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form MONDO_0017696
sclerosing perineurioma MONDO_0015030
glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form MONDO_0017697
glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form MONDO_0017698
Teebi hypertelorism syndrome 2 MONDO_0030674
lissencephaly with cerebellar hypoplasia type C MONDO_0015036