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Mondo Disease Ontology
MONDO
All terms in MONDO
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Label
Id
Description
Kleine-Levin syndrome
MONDO_0007863
viral dilated cardiomyopathy
MONDO_0005200
angioosteohypertrophic syndrome
MONDO_0007864
atopic IgE-mediated allergic disorder
MONDO_0005202
isolated cloverleaf skull syndrome
MONDO_0007861
Waardenburg syndrome type 3
MONDO_0007862
focal palmoplantar and gingival keratoderma
MONDO_0007860
immunodeficiency 57
MONDO_0020849
obsolete congenital thyroid malformation without hypothyroidism
MONDO_0019859
osteopetrosis, autosomal dominant 3
MONDO_0020848
autosomal dominant osteopetrosis
MONDO_0020645
intellectual disability, autosomal dominant 58
MONDO_0020847
intellectual disability, autosomal recessive 64
MONDO_0020846
obsolete primary congenital hypothyroidism without thyroid developmental anomaly
MONDO_0019856
progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5
MONDO_0020845
athyreosis
MONDO_0019855
idiopathic congenital hypothyroidism
MONDO_0019858
pseudomembranous diphtheritic conjunctivitis
MONDO_0020843
pseudomembranous conjunctivitis
MONDO_0001217
congenital hypothyroidism due to transplacental passage of maternal TSH-binding inhibitory antibodies
MONDO_0019857