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All terms in MONDO

Label Id Description
epithelioid trophoblastic tumor MONDO_0016787
gestational trophoblastic neoplasm MONDO_0018944
obsolete autosomal recessive limb-girdle muscular dystrophy type 2R MONDO_0014129
obsolete genetic hyperferritinemia without iron overload MONDO_0016788
pyruvate metabolism disorder MONDO_0016789
inborn disorder of energy metabolism MONDO_0019243
TCF12-related craniosynostosis MONDO_0014128
paternal 14q32.2 hypomethylation syndrome MONDO_0016782
motor developmental delay due to 14q32.2 paternally expressed gene defect MONDO_0014541
maternal 14q32.2 hypermethylation syndrome MONDO_0016783
obsolete gestational trophoblastic disease MONDO_0016784
complete hydatidiform mole MONDO_0016785
primary ciliary dyskinesia 21 MONDO_0014123
myofibromatosis, infantile, 2 MONDO_0014122
infantile myofibromatosis MONDO_0016824
autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures MONDO_0014121
paternal 14q32.2 microdeletion syndrome MONDO_0016780
maternal 14q32.2 microdeletion syndrome MONDO_0016781
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A13 MONDO_0014120
reproductive system cancer MONDO_0002149