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All terms in MONDO

Label Id Description
ganglioneuroma MONDO_0005033
obsolete gangliocytoma MONDO_0002294
macrocephaly-developmental delay syndrome MONDO_0014289
short-rib thoracic dysplasia 10 with or without polydactyly MONDO_0014284
autosomal dominant nonsyndromic hearing loss 56 MONDO_0014283
hereditary spastic paraplegia 72 MONDO_0014282
pure hereditary spastic paraplegia MONDO_0015149
cholangiocarcinoma, susceptibility to MONDO_0014281
cholangiocarcinoma MONDO_0019087
Joubert syndrome 21 MONDO_0014288
short-rib thoracic dysplasia 11 with or without polydactyly MONDO_0014287
neuropathy, hereditary sensory, type 1F MONDO_0014286
congenital dyserythropoietic anemia type type 1B MONDO_0014285
congenital dyserythropoietic anemia type 1 MONDO_0020337
immunodeficiency 19 MONDO_0014280
staphylococcus aureus pneumonia MONDO_0041879
staphylococcal pneumonia MONDO_0005970
hereditary spastic paraplegia 57 MONDO_0014295
chromosome 15q11.2 deletion syndrome MONDO_0014294
autosomal dominant nonsyndromic hearing loss 58 MONDO_0014293