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Mondo Disease Ontology
MONDO
All terms in MONDO
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Label
Id
Description
premature ovarian failure 6
MONDO_0012861
attention deficit-hyperactivity disorder, susceptibility to, 5
MONDO_0012862
Wilson disease
MONDO_0010200
thrombophilia due to protein C deficiency, autosomal recessive
MONDO_0012860
hereditary thrombophilia due to congenital protein C deficiency
MONDO_0019145
Pseudofolliculitis barbae
MONDO_0012865
obsolete Wiskott-Aldrich syndrome
MONDO_0010202
hereditary spastic paraplegia 35
MONDO_0012866
Winchester syndrome
MONDO_0010201
lysosomal acid lipase deficiency
MONDO_0010204
attention deficit-hyperactivity disorder, susceptibility to, 6
MONDO_0012863
chromosome 2q32-q33 deletion syndrome
MONDO_0012864
intellectual disability, Wolff type
MONDO_0010203
cytomegalovirus retinitis
MONDO_0000878
viral eye infection
MONDO_0020950
obsolete Cryptococcal meningitis
MONDO_0000877
obsolete myeloid neoplasms associated with PDGFRB rearrangement
MONDO_0000883
obsolete myeloid and lymphoid neoplasms associated with PDGFRA rearrangement
MONDO_0000882
obsolete myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1
MONDO_0000881
obsolete lupus nephritis
MONDO_0000880