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Mondo Disease Ontology
MONDO
All terms in MONDO
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Label
Id
Description
chronic neurovisceral acid sphingomyelinase deficiency
MONDO_0850058
hereditary persistence of fetal hemoglobin-intellectual disability syndrome
MONDO_0850059
submucosal cleft palate
MONDO_0015479
pinnae fistula or cyst
MONDO_0015477
congenital aphakia-iris hypoplasia-microphthalmia-microcornea syndrome
MONDO_0850050
obsolete cryptococcosis
MONDO_0015472
benign focal seizures of adolescence
MONDO_0015471
F12-associated cold autoinflammatory syndrome
MONDO_0850053
hemophilia B leyden
MONDO_0850054
obsolete rare head and neck malformation
MONDO_0015475
cryptosporidiosis
MONDO_0015474
cryptorchidism-arachnodactyly-intellectual disability syndrome
MONDO_0015473
obsolete gallbladder squamous cell carcinoma
MONDO_0003498
sarcomatoid squamous cell skin carcinoma
MONDO_0003499
ovarian squamous cell carcinoma
MONDO_0003494
ovarian squamous cell neoplasm
MONDO_0003495
autosomal recessive cutis laxa type 2C
MONDO_0027462
obsolete endometrial squamous cell carcinoma
MONDO_0003496
renal pelvis squamous cell carcinoma
MONDO_0003497
ampulla of vater squamous cell carcinoma
MONDO_0003490