MONDO_merge Find_IDs Find_Terms Annotation
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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
acute bronchitis and bronchiolitis 3781
desmin-related, with arrhythmogenic right ventricular cardiomyopathy myopathy C563784
congenital dyserythropoietic anemia, and neutrophilic dermatosis chronic recurrent multifocal osteomyelitis C537839
familial, 7 arrhythmogenic right ventricular dysplasia C563784
intellectual disability, autosomal recessive 34 13785
larsen syndrome, autosomal dominant C537873
hyperthyroidism, nonautoimmune, autosomal dominant C563786
ectodermal dysplasia, and lacrimal duct abnormality Tetra-amelia C537838
mental retardation and multiple dysmorphisms short stature C537887
foveal hypoplasia and presenile cataract syndrome C537858
mental retardation, autosomal recessive 34 13785
intellectual disability, autosomal recessive 34, with variant lissencephaly 13785
mental retardation, autosomal recessive 34, with variant lissencephaly 13785
mental retardation, autosomal recessive 34, with variant lissencephaly; MRT34 http://purl.obolibrary.org/obo/MONDO_0013785
mental retardation, autosomal recessive 34; MRT34 http://purl.obolibrary.org/obo/MONDO_0013785