All terms in MONDO
| Label |
Id |
Description |
|
obsolete apricot allergy
|
MONDO_0000780 |
|
|
congenital sucrase-isomaltase deficiency
|
MONDO_0009114 |
|
|
hemolytic anemia due to diphosphoglycerate mutase deficiency
|
MONDO_0009113 |
|
|
rhizomelic chondrodysplasia punctata type 2
|
MONDO_0009112 |
|
|
dihydropyrimidinuria
|
MONDO_0009111 |
|
|
von Voss-Cherstvoy syndrome
|
MONDO_0009121 |
|
|
Hunter-Macdonald syndrome
|
MONDO_0012773 |
|
|
tetraamelia-multiple malformations syndrome
|
MONDO_0010110 |
|
|
diverticulosis of bowel, hernia, and retinal detachment
|
MONDO_0009120 |
|
|
chromosome 15q13.3 microdeletion syndrome
|
MONDO_0012774 |
|
|
asthma-related traits, susceptibility to, 7
|
MONDO_0012771 |
|
|
thalamic degeneration, symmetric infantile
|
MONDO_0010112 |
|
|
Stevenson-Carey syndrome
|
MONDO_0012772 |
|
|
odontotrichomelic syndrome
|
MONDO_0010111 |
|
|
celiac disease, susceptibility to, 8
|
MONDO_0012777 |
|
|
thanatophoric dysplasia, Glasgow variant
|
MONDO_0010114 |
|
|
celiac disease, susceptibility to, 9
|
MONDO_0012778 |
|
|
obsolete thalidomide susceptibility
|
MONDO_0010113 |
|
|
thoracomelic dysplasia
|
MONDO_0010116 |
|
|
thrombocytopenia 4
|
MONDO_0012775 |
|
