| mondo_id | mondo_label | xref | xref_source | original_label | definition | parents |
|---|---|---|---|---|---|---|
| ID | LABEL | A oboInOwl:hasDbXref | >A oboInOwl:source SPLIT= | A IAO:0000115 | ||
| MONDO:0970943 | spermatogenic failure, x-linked, 8 | OMIM:301119 | MONDO:equivalentTo | spermatogenic failure, x-linked, 8 | ||
| MONDO:0970944 | leigh syndrome, mitochondrial | OMIM:500017 | MONDO:equivalentTo | leigh syndrome, mitochondrial | ||
| MONDO:0970945 | developmental and epileptic encephalopathy 116 | OMIM:620806 | MONDO:equivalentTo | developmental and epileptic encephalopathy 116 | MONDO:0100062 | |
| MONDO:0970946 | mhc class 2 deficiency 2 | OMIM:620815 | MONDO:equivalentTo | mhc class 2 deficiency 2 | ||
| MONDO:0970947 | mhc class 2 deficiency 3 | OMIM:620816 | MONDO:equivalentTo | mhc class 2 deficiency 3 | ||
| MONDO:0970948 | mhc class 2 deficiency 4 | OMIM:620817 | MONDO:equivalentTo | mhc class 2 deficiency 4 | ||
| MONDO:0970949 | mhc class 2 deficiency 5 | OMIM:620818 | MONDO:equivalentTo | mhc class 2 deficiency 5 | ||
| MONDO:0970950 | rothmund-thomson syndrome, type 4 | OMIM:620819 | MONDO:equivalentTo | rothmund-thomson syndrome, type 4 | MONDO:0010002 | |
| MONDO:0970951 | el hayek-chahrour neurodevelopmental syndrome | OMIM:620820 | MONDO:equivalentTo | el hayek-chahrour neurodevelopmental syndrome | ||
| MONDO:0970952 | spermatogenic failure 91 | OMIM:620838 | MONDO:equivalentTo | spermatogenic failure 91 | ||
| MONDO:0970953 | amyloidosis, hereditary systemic | OMIMPS:105210 | MONDO:equivalentTo | Amyloidosis, hereditary systemic | ||
| MONDO:0970954 | mhc class i deficiency | OMIMPS:604571 | MONDO:equivalentTo | MHC class I deficiency | ||
| MONDO:0970955 | neuroocular syndrome | OMIMPS:619539 | MONDO:equivalentTo | Neuroocular syndrome |