Id |
Subject |
Object |
Predicate |
Lexical cue |
mondo_id |
T1 |
62-76 |
DiseaseOrPhenotypicFeature |
denotes |
microphthalmia |
0021129 |
T2 |
78-90 |
DiseaseOrPhenotypicFeature |
denotes |
microcephaly |
0001149 |
T3 |
491-505 |
DiseaseOrPhenotypicFeature |
denotes |
microphthalmia |
0021129 |
T4 |
507-514 |
DiseaseOrPhenotypicFeature |
denotes |
choroid |
0001280 |
T5 |
515-523 |
DiseaseOrPhenotypicFeature |
denotes |
coloboma |
0001476 |
T6 |
525-537 |
DiseaseOrPhenotypicFeature |
denotes |
microcephaly |
0001149 |
T7 |
539-555 |
DiseaseOrPhenotypicFeature |
denotes |
renal hypoplasia |
0019637 |
T8 |
569-579 |
DiseaseOrPhenotypicFeature |
denotes |
paraplegia |
0003757 |
T9 |
820-834 |
DiseaseOrPhenotypicFeature |
denotes |
microphthalmia |
0021129 |
T10 |
1230-1265 |
DiseaseOrPhenotypicFeature |
denotes |
Hamel cerebropalatocardiac syndrome |
0019767 |
T11 |
1330-1339 |
DiseaseOrPhenotypicFeature |
denotes |
mosaicism |
0700062 |
T12 |
1549-1563 |
DiseaseOrPhenotypicFeature |
denotes |
microphthalmia |
0021129 |