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All terms in MONDO

Label Id Description
obsolete hepatic veno-occlusive disease MONDO_0000887
obsolete meningococcal meningitis MONDO_0000886
fascial dystrophy, congenital MONDO_0009219
obsolete cloacal exstrophy MONDO_0000885
myeloid and lymphoid neoplasms associated with FGFR1 abnormalities MONDO_0000884
myeloid/lymphoid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB, FGFR1 or JAK2 MONDO_0015688
Farber lipogranulomatosis MONDO_0009218
primary CD59 deficiency MONDO_0012858
Fanconi-like syndrome MONDO_0009217
autosomal recessive osteopetrosis 7 MONDO_0012859
glycogen storage disease due to GLUT2 deficiency MONDO_0009216
Birk-Barel syndrome MONDO_0012856
Fanconi anemia complementation group A MONDO_0009215
porokeratosis 5, disseminated superficial actinic type MONDO_0012857
Fanconi anemia complementation group D2 MONDO_0009214
Fanconi anemia complementation group C MONDO_0009213
congenital factor X deficiency MONDO_0009212
congenital factor VII deficiency MONDO_0009211
congenital factor V deficiency MONDO_0009210
factor V deficiency MONDO_0020586