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created at 2021-12-22 03:08:20 UTC
updated at 2021-12-22 07:06:09 UTC
MONDO_bioport_pref_name
183,974 entries
Label
Id
neurodegeneration with brain iron accumulation due to C19orf12 mutation 13674
neurodegeneration with brain iron accumulation type 4 13674
subendocardial myocardial infarction 3674
osteosclerosis, autosomal dominant worth type with torus palatinus C536748
severe intrauterine growth retardation with increased mitomycin c sensitivity C536744
congenital woolly hair C536745
benign hyperostosis corticalis generalisata C536748
hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome C536742
x-linked immunoneurologic disorder C536743
woolly hair, congenital C536745
hyperostosis corticalis generalisata congenita C536748
hyperostosis corticalis generalisata, benign form of worth, with torus palatinus C536748
woolly hair, hypotrichosis, everted lower lip and outstanding ears C536746
woolly hair, hypotrichosis, everted lower lip, and outstanding ears C536746
benign form of worth, with torus palatinus hyperostosis corticalis generalisata C536748