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
retinitis pigmentosa 63 13780
retinitis pigmentosa 63; RP63 http://purl.obolibrary.org/obo/MONDO_0013780
retinitis pigmentosa 64 13786
pseudohypoaldosteronism, type IID 13781
pseudohypoaldosteronism, type IID; PHA2D http://purl.obolibrary.org/obo/MONDO_0013781
pseudohypoaldosteronism, type IIE 13782
pseudohypoaldosteronism, type IIE; PHA2E http://purl.obolibrary.org/obo/MONDO_0013782
intellectual disability, autosomal recessive 34 13785
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
intellectual disability, autosomal recessive type 34 13785
mental retardation, autosomal recessive type 34 13785