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All terms in MONDO

Label Id Description
hereditary angioedema type 2 MONDO_0015054
hereditary angioedema type 1 MONDO_0015053
myopia 28, autosomal recessive MONDO_0030697
obsolete primary interstitial lung disease specific to childhood due to pulmonary surfactant protein anomalies MONDO_0015052
mitochondrial DNA depletion syndrome 20 (mngie type) MONDO_0030696
tubular duplication of the esophagus MONDO_0015051
obsolete Waterhouse-Friderichsen syndrome MONDO_0015058
pulmonary fibrosis and/or bone marrow failure, telomere-related, 6 MONDO_0030690
immunodeficiency 96 MONDO_0030693
acquired angioedema type 1 MONDO_0015056
immunodeficiency 95 MONDO_0030692
acquired angioedema type 2 MONDO_0015055
spermatogenic failure 18 MONDO_0054615
esophageal duplication cyst MONDO_0015050
Charcot-Marie-Tooth disease, demyelinating, IIA 1H MONDO_0030689
unilateral retinoblastoma MONDO_0003076
deafness, Y-linked 2 MONDO_0027048
trilateral retinoblastoma MONDO_0003073
obsolete familial retinoblastoma MONDO_0003074
bilateral retinoblastoma MONDO_0003075