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Mondo Disease Ontology
MONDO
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Label
Id
Description
Sammartino-Decreccio syndrome
MONDO_0042600
Samson-Gardner syndrome
MONDO_0042601
Samson-Viljoen syndrome
MONDO_0042602
Sanderson-Fraser syndrome
MONDO_0042603
disorder of beta and omega amino acid metabolism
MONDO_0017684
hypotonia, ataxia, and delayed development syndrome
MONDO_0015021
intellectual disability, autosomal recessive 59
MONDO_0015020
vitamin B12-responsive methylmalonic acidemia, type cblDv2
MONDO_0017685
disorder of neutral amino acid transport
MONDO_0017687
developmental and epileptic encephalopathy, 51
MONDO_0015025
obsolete autosomal recessive disease associated with punctate palmoplantar keratoderma as a major feature
MONDO_0017680
ectodermal dysplasia 12, hypohidrotic/hair/tooth/nail type
MONDO_0015024
erythrokeratoderma variabilis progressiva
MONDO_0017681
MYPN-related myopathy
MONDO_0015023
intellectual disability-polydactyly-uncombable hair syndrome
MONDO_0017682
methylcobalamin deficiency type cblDv1
MONDO_0017683
intellectual developmental disorder with dysmorphic facies and ptosis
MONDO_0015022
thymic large cell neuroendocrine carcinoma
MONDO_0003047
obsolete type C thymoma
MONDO_0003048
ovarian large-cell neuroendocrine carcinoma
MONDO_0003049