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Mondo Disease Ontology
MONDO
All terms in MONDO
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Label
Id
Description
tonsil squamous cell carcinoma
MONDO_0000535
isolated glycerol kinase deficiency
MONDO_0018459
inborn glycerol kinase deficiency
MONDO_0010613
has an isolated presentation
MONDO_0021128
familial hypocalciuric hypercalcemia
MONDO_0018458
hypercalcemia disease
MONDO_0001566
interstitial lung disease specific to childhood
MONDO_0017014
endocrine system disorder
MONDO_0005151
obsolete dysostosis of genetic origin with limb anomaly as a major feature
MONDO_0018455
dysostosis of genetic origin
MONDO_0018454
dysostosis
MONDO_0018234
obsolete rare genetic bone development disorder
MONDO_0018457
polyarticular juvenile idiopathic arthritis
MONDO_0018456
juvenile idiopathic arthritis
MONDO_0011429
X-linked distal hereditary motor neuropathy
MONDO_0018451
distal hereditary motor neuropathy
MONDO_0018894
spinal muscular atrophy with respiratory distress type 2
MONDO_0018450
familial atypical multiple mole melanoma syndrome
MONDO_0018453
inherited skin tumor
MONDO_0015950
obsolete deficiency of the interleukin-36 receptor antagonist
MONDO_0018452