All terms in MONDO
| Label |
Id |
Description |
|
X-linked lymphoproliferative disease due to XIAP deficiency
|
MONDO_0010385 |
|
|
hyperostosis corticalis generalisata
|
MONDO_0009395 |
|
|
hypospadias 1, X-linked
|
MONDO_0010384 |
|
|
juvenile Paget disease
|
MONDO_0009394 |
|
|
obsolete invasive pneumococcal disease, recurrent isolated, 2
|
MONDO_0010387 |
|
|
ornithine translocase deficiency
|
MONDO_0009393 |
|
|
immunodeficiency 33
|
MONDO_0010386 |
|
|
hyperopia, high
|
MONDO_0009392 |
|
|
X-linked Mendelian susceptibility to mycobacterial diseases due to CYBB deficiency
|
MONDO_0010389 |
|
|
hypermetabolism due to defect in mitochondria
|
MONDO_0009391 |
|
|
rolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked
|
MONDO_0010388 |
|
|
rolandic epilepsy-speech dyspraxia syndrome
|
MONDO_0015587 |
|
|
hyperlysinuria with hyperammonemia
|
MONDO_0009390 |
|
|
Tn polyagglutination syndrome
|
MONDO_0010381 |
|
|
cataract, ataxia, short stature, and intellectual disability
|
MONDO_0010380 |
|
|
fragile X-associated tremor/ataxia syndrome
|
MONDO_0010382 |
|
|
hyperphosphatemia, polyuria, and seizures
|
MONDO_0009399 |
|
|
hyperphosphatasia with intellectual disability syndrome 1
|
MONDO_0009398 |
|
|
neonatal severe primary hyperparathyroidism
|
MONDO_0009397 |
|
|
developmental and epileptic encephalopathy, 2
|
MONDO_0010396 |
|
