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All terms in MONDO

Label Id Description
muscular dystrophy-white matter spongiosis syndrome MONDO_0015994
Charcot-Marie-Tooth disease recessive intermediate B MONDO_0013338
dilated cardiomyopathy 1GG MONDO_0013339
chromosome 19p13.13 deletion syndrome MONDO_0013336
neuropathy, hereditary sensory and autonomic, type 1C MONDO_0013337
agenesis of the corpus callosum and congenital lymphedema MONDO_0013330
factor 5 and Factor VIII, combined deficiency of, 2 MONDO_0013331
obsolete progressive cone dystrophy MONDO_0015992
iron deficiency anemia MONDO_0001356
ocular siderosis MONDO_0001355
obsolete acute endophthalmitis MONDO_0001354
Bordetella parapertussis infectious disease MONDO_0001353
obsolete Kohler disease MONDO_0001359
familial clubfoot due to 17q23.1q23.2 microduplication MONDO_0013329
round ligament malignant neoplasm MONDO_0001352
uterine adnexa cancer MONDO_0001351
parametrium malignant neoplasm MONDO_0001350
broad ligament malignant neoplasm MONDO_0001108
obsolete superimposed infection MONDO_0040964
d-2-hydroxyglutaric aciduria 2 MONDO_0013345