Id |
Subject |
Object |
Predicate |
Lexical cue |
mondo_id |
T2 |
21-31 |
DiseaseOrPhenotypicFeature |
denotes |
congenital |
0021140 |
T1 |
21-57 |
DiseaseOrPhenotypicFeature |
denotes |
congenital generalized lipodystrophy |
0006536 |
T3 |
32-57 |
DiseaseOrPhenotypicFeature |
denotes |
generalized lipodystrophy |
0027766 |
T4 |
44-57 |
DiseaseOrPhenotypicFeature |
denotes |
lipodystrophy |
0006573 |
T5 |
116-152 |
DiseaseOrPhenotypicFeature |
denotes |
Congenital generalized lipodystrophy |
0006536 |
T6 |
127-152 |
DiseaseOrPhenotypicFeature |
denotes |
generalized lipodystrophy |
0027766 |
T7 |
139-152 |
DiseaseOrPhenotypicFeature |
denotes |
lipodystrophy |
0006573 |
T8 |
164-168 |
DiseaseOrPhenotypicFeature |
denotes |
rare |
0021136 |
T9 |
169-196 |
DiseaseOrPhenotypicFeature |
denotes |
autosomal recessive disease |
0006025 |
T10 |
229-237 |
DiseaseOrPhenotypicFeature |
denotes |
complete |
0700063 |
T11 |
507-521 |
DiseaseOrPhenotypicFeature |
denotes |
cardiomyopathy |
0004994 |
T12 |
662-671 |
DiseaseOrPhenotypicFeature |
denotes |
xanthomas |
0005236 |
T13 |
685-705 |
DiseaseOrPhenotypicFeature |
denotes |
hypertriglyceridemia |
0005347 |
T14 |
916-923 |
DiseaseOrPhenotypicFeature |
denotes |
hepatic |
0002251 |
T15 |
1006-1020 |
DiseaseOrPhenotypicFeature |
denotes |
cardiomyopathy |
0004994 |