Terminology Service for NFDI4Health
All terms in CLO
| Label | Id | Description |
|---|---|---|
| GM17822 cell | CLO_0016514 | [ PANTOTHENATE KINASE-ASSOCIATED NEURODEGENERATION; PKAN; HALLERVORDEN-SPATZ DISEASE INCLUDED PANTOTHENATE KINASE 2; PANK2] |
| Hallervorden-Spatz syndrome | DOID_3981 | |
| GM17825 cell | CLO_0016517 | [ HUMAN VARIATION PANEL - HAN PEOPLE OF LOS ANGELES PANEL OF 100] |
| GM17824 cell | CLO_0016516 | [ HUMAN VARIATION PANEL - HAN PEOPLE OF LOS ANGELES PANEL OF 100] |
| gestational diabetes complicating pregnancy, childbirth, or the puerperium | DOID_1550 | |
| GM17833 cell | CLO_0016519 | [ HUMAN VARIATION PANEL - HAN PEOPLE OF LOS ANGELES PANEL OF 100] |
| GM17826 cell | CLO_0016518 | [ HUMAN VARIATION PANEL - HAN PEOPLE OF LOS ANGELES PANEL OF 100] |
| GM17818 cell | CLO_0016511 | [ HUMAN VARIATION PANEL - HAN PEOPLE OF LOS ANGELES PANEL OF 100] |
| GM17817 cell | CLO_0016510 | [ HUMAN VARIATION PANEL - HAN PEOPLE OF LOS ANGELES PANEL OF 100] |
| IGF008/99 cell | CLO_0004546 | |
| IGF009/00 cell | CLO_0004547 | |
| IGF008/97 cell | CLO_0004544 | |
| IGF008/98 cell | CLO_0004545 | |
| IGF009/01 cell | CLO_0004548 | |
| IGF009/77 cell | CLO_0004549 | |
| axilla | UBERON_0009472 | |
| myotonic dystrophy | DOID_11722 | |
| muscular dystrophy | EFO_0000757 | [A heterogeneous group of inherited MYOPATHIES, characterized by wasting and weakness of the SKELETAL MUSCLE. They are categorized by the sites of MUSCLE WEAKNESS; AGE OF ONSET; and INHERITANCE PATTERNS.] |
| myotonic disorder | DOID_450 | |
| glycogen storage disease type VII | DOID_11721 |