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Mondo Disease Ontology
MONDO
All terms in MONDO
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Label
Id
Description
hydrocephaly-tall stature-joint laxity syndrome
MONDO_0009363
intellectual disability, X-linked 82
MONDO_0010352
growth delay-hydrocephaly-lung hypoplasia syndrome
MONDO_0009362
Fanconi anemia complementation group B
MONDO_0010351
autosomal recessive hydrocephalus due to congenital stenosis of aqueduct of Sylvius
MONDO_0009361
Allan-Herndon-Dudley syndrome
MONDO_0010354
hydrocephalus, nonsyndromic, autosomal recessive 1
MONDO_0009360
deafness-intellectual disability, Martin-Probst type syndrome
MONDO_0010353
nephrogenic syndrome of inappropriate antidiuresis
MONDO_0010356
syndromic X-linked intellectual disability Claes-Jensen type
MONDO_0010355
hypophosphatemic rickets, X-linked recessive
MONDO_0010358
obsolete MRX78
MONDO_0010357
hair defect with photosensitivity and intellectual disability syndrome
MONDO_0022316
premature ovarian failure 2A
MONDO_0010350
salmonella infections, animal
MONDO_0024982
rodent disease
MONDO_0024981
2-methylacetoacetyl CoA thiolase deficiency
MONDO_0022321
2-hydroxyethyl methacrylate sensitization
MONDO_0022323
obsolete genetic urogenital tract malformation
MONDO_0024987
MONDO_0022326
MONDO_0022326