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Mondo Disease Ontology
MONDO
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Label
Id
Description
ring chromosome 13
MONDO_0019907
ring chromosome 16
MONDO_0019909
X small rings
MONDO_0019926
paternal uniparental disomy of chromosome 21
MONDO_0019925
48,XXXY syndrome
MONDO_0019928
paternal uniparental disomy of chromosome 7
MONDO_0019922
paternal uniparental disomy of chromosome 6
MONDO_0019921
paternal uniparental disomy of chromosome 20
MONDO_0019924
Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11
MONDO_0019923
paternal uniparental disomy of chromosome 5
MONDO_0019920
malignant hyperthermia, susceptibility to, 2
MONDO_0007939
marfanoid hypermobility syndrome
MONDO_0007948
Marshall syndrome
MONDO_0007949
Marfan syndrome
MONDO_0007947
Treacher Collins syndrome 1
MONDO_0007944
mannose 6-phosphate receptor recognition defect, Lebanese type
MONDO_0007945
Mammastatin
MONDO_0007942
Nager acrofacial dysostosis
MONDO_0007943
malignant hyperthermia, susceptibility to, 3
MONDO_0007940
malocclusion due to protuberant upper front teeth
MONDO_0007941