Terminology Service for NFDI4Health
All terms in CLO
| Label | Id | Description |
|---|---|---|
| GM12133 cell | CLO_0019100 | [ ALAGILLE SYNDROME; AGS] |
| ND13813 cell | CLO_0034746 | [ POPULATION/CONVENIENCE CONTROL] |
| DA05118 cell | CLO_0010775 | [ DIABETES MELLITUS FAMILY SAMPLE] |
| GM12132 cell | CLO_0019101 | [ ALAGILLE SYNDROME; AGS] |
| DA05123 cell | CLO_0010772 | [ DIABETES MELLITUS FAMILY SAMPLE] |
| GM12129 cell | CLO_0019106 | [ MYASTHENIA GRAVIS; MG] |
| ND13811 cell | CLO_0034740 | [ SPOUSAL CONTROL] |
| GM12127 cell | CLO_0019107 | [ CIRRHOSIS, FAMILIAL CIRRHOSIS, FAMILIAL, WITH PULMONARY HYPERTENSION, INCLUDED] |
| DA05119 cell | CLO_0010773 | [ DIABETES MELLITUS FAMILY SAMPLE] |
| ND13810 cell | CLO_0034741 | [ SPOUSAL CONTROL] |
| HQ00637 cell | CLO_0010770 | [ HUNTINGTON DISEASE; HD] |
| GM12136 cell | CLO_0019104 | [ GLYCOGEN STORAGE DISEASE IV] |
| ND13809 cell | CLO_0034742 | [ ALS PANEL; UPPER-LIMB ONSET; DEFINITE AND PROBABLE ALS AMYOTROPHIC LATERAL SCLEROSIS] |
| DA05124 cell | CLO_0010771 | [ DIABETES MELLITUS FAMILY SAMPLE] |
| GM12135 cell | CLO_0019105 | [ PRADER-WILLI SYNDROME; PWS] |
| ND13842 cell | CLO_0034736 | [ POPULATION/CONVENIENCE CONTROL] |
| GM12147 cell | CLO_0019120 | [ CEPH/UTAH PEDIGREE 1408] |
| GM12144 cell | CLO_0019121 | [ CYTOCHROME P450, SUBFAMILY IIC, POLYPEPTIDE 19; CYP2C19 CEPH/UTAH PEDIGREE 1334 INTERNATIONAL HAPMAP PROJECT - CEPH (PLATE I) [UTAH RESIDENTS WITH ANCESTRY FROM NORTHERN AND WESTERN EUROPE]] |
| ND13806 cell | CLO_0034737 | [ PARKINSON'S DISEASE] |
| GM09058 cell | CLO_0010789 | [ USHER SYNDROME, TYPE IA; USH1A] |