All terms in MONDO
| Label |
Id |
Description |
|
Lyme disease
|
MONDO_0019632 |
|
|
mitochondrial complex 1 deficiency, nuclear type 6
|
MONDO_0032611 |
|
|
familial nasal acilia
|
MONDO_0019634 |
|
|
relapsing fever
|
MONDO_0019633 |
|
|
congenital ectropion uveae
|
MONDO_0019630 |
|
|
vertebral anomalies and variable endocrine and T-cell dysfunction
|
MONDO_0032607 |
|
|
mitochondrial complex 1 deficiency, nuclear type 3
|
MONDO_0032608 |
|
|
intellectual disability, autosomal recessive 66
|
MONDO_0032605 |
|
|
mitochondrial complex 1 deficiency, nuclear type 2
|
MONDO_0032606 |
|
|
obsolete spitz nevus
|
MONDO_0007658 |
|
|
polydactyly, postaxial, type A9
|
MONDO_0032603 |
|
|
obsolete giant platelet syndrome with thrombocytopenia
|
MONDO_0007659 |
|
|
retinitis pigmentosa 84
|
MONDO_0032604 |
|
|
Gerstmann-Straussler-Scheinker syndrome
|
MONDO_0007656 |
|
|
inflammatory bowel disease, immunodeficiency, and encephalopathy
|
MONDO_0032601 |
|
|
giant neutrophil leukocytes
|
MONDO_0007657 |
|
|
genu valgum, st. Helena familial
|
MONDO_0007654 |
|
|
epileptic encephalopathy, infantile or early childhood, 3
|
MONDO_0020632 |
|
|
fissured tongue
|
MONDO_0007655 |
|
|
epileptic encephalopathy, infantile or early childhood, 2
|
MONDO_0020631 |
|
