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Mondo Disease Ontology
MONDO
All terms in MONDO
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Label
Id
Description
Brill-Zinsser disease
MONDO_0005680
bronchopneumonia
MONDO_0005682
obsolete orofaciodigital syndrome
MONDO_0003020
obsolete MONDO:0005681
MONDO_0005681
ichthyosis, congenital, autosomal recessive 12
MONDO_0015018
anterior segment dysgenesis 8
MONDO_0015017
anterior segment dysgenesis 6
MONDO_0015016
congenital bile acid synthesis defect 6
MONDO_0015015
focal acral hyperkeratosis
MONDO_0017677
obsolete obsolete disease with punctate palmoplantar keratoderma as a major feature
MONDO_0017678
obsolete obsolete autosomal dominant disease associated with punctate palmoplantar keratoderma as a major feature
MONDO_0017679
Yao syndrome
MONDO_0015019
atypical glycine encephalopathy
MONDO_0015010
glycine encephalopathy
MONDO_0011612
obsolete disease with focal palmoplantar keratoderma as a major feature
MONDO_0017674
coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness
MONDO_0015014
retinitis pigmentosa 77
MONDO_0015013
mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders
MONDO_0015012
obsolete autosomal recessive disease with diffuse palmoplantar keratoderma as a major feature
MONDO_0017671
optic atrophy 11
MONDO_0015011