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Mondo Disease Ontology
MONDO
All terms in MONDO
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Label
Id
Description
obsolete amyloidosis nodular localized cutaneous
MONDO_0022446
epsilon-trimethyllysine hydroxylase deficiency
MONDO_0010469
hereditary palmoplantar keratoderma, Gamborg-Nielsen type
MONDO_0009489
keratoconus posticus circumscriptus
MONDO_0009488
keratoconus and congenital hip dysplasia
MONDO_0009487
autosomal recessive Kenny-Caffey syndrome
MONDO_0009486
oculocerebrofacial syndrome, Kaufman type
MONDO_0009485
Keutel syndrome
MONDO_0009495
hearing loss, X-linked 6
MONDO_0010484
X-linked nonsyndromic hearing loss
MONDO_0019586
obsolete Ketoadipicaciduria
MONDO_0009494
X-linked intellectual disability, Cantagrel type
MONDO_0010483
Richards-Rundle syndrome
MONDO_0009493
Olmsted syndrome, X-linked
MONDO_0010486
succinyl-CoA:3-ketoacid CoA transferase deficiency
MONDO_0009492
X-linked colobomatous microphthalmia-microcephaly-intellectual disability-short stature syndrome
MONDO_0010485
Haim-Munk syndrome
MONDO_0009491
intellectual disability, X-linked 100
MONDO_0010488
Papillon-Lefevre disease
MONDO_0009490
intellectual disability, X-linked 99
MONDO_0010487