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All terms in MONDO

Label Id Description
maternal uniparental disomy of chromosome 22 MONDO_0019919
maternal uniparental disomy of chromosome 21 MONDO_0019918
obsolete rare gynecologic or obstetric disease MONDO_0019937
obsolete rare otorhinolaryngological malformation MONDO_0019936
early-onset schizophrenia MONDO_0019939
acromegaly MONDO_0019933
isolated partial vaginal agenesis MONDO_0019932
escherichia coli infection MONDO_0020920
Leydig cell hypoplasia due to partial LH resistance MONDO_0019931
Leydig cell hypoplasia due to complete LH resistance MONDO_0019930
corneal dystrophy, Meesmann, 2 MONDO_0032904
spastic paraplegia 81, autosomal recessive MONDO_0032905
mediosternal depigmentation line MONDO_0007957
Joubert syndrome 36 MONDO_0032902
familial medullary thyroid carcinoma MONDO_0007958
arthrogryposis multiplex congenita 4, neurogenic, with agenesis of the corpus callosum MONDO_0032903
Meckel diverticulum MONDO_0007955
neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movements MONDO_0032900
Pai syndrome MONDO_0007956
Catifa syndrome MONDO_0032901