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Mondo Disease Ontology
MONDO
All terms in MONDO
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Label
Id
Description
microform holoprosencephaly
MONDO_0017219
alobar holoprosencephaly
MONDO_0019757
lobar holoprosencephaly
MONDO_0019756
septopreoptic holoprosencephaly
MONDO_0017218
midline interhemispheric variant of holoprosencephaly
MONDO_0019758
Fanconi anemia complementation group V
MONDO_0014985
lung disease, immunodeficiency, and chromosome breakage syndrome;
MONDO_0014984
lethal acantholytic epidermolysis bullosa
MONDO_0012323
suprabasal epidermolysis bullosa simplex
MONDO_0015550
congenital myasthenic syndrome 21
MONDO_0014983
migraine, familial hemiplegic, 3
MONDO_0012320
Alzheimer disease 10
MONDO_0012321
early-onset autosomal dominant Alzheimer disease
MONDO_0015140
myopia 25, autosomal dominant
MONDO_0014982
uncombable hair syndrome 2
MONDO_0014989
autosomal recessive nonsyndromic hearing loss 42
MONDO_0012326
autosomal recessive nonsyndromic hearing loss 46
MONDO_0012327
obsolete 3-methylglutaconic aciduria, type VIII
MONDO_0014988
Fanconi anemia complementation group U
MONDO_0014987
Frias syndrome
MONDO_0012324