All terms in MONDO
| Label |
Id |
Description |
|
chylomicron retention disease
|
MONDO_0009528 |
|
|
lipase deficiency, combined
|
MONDO_0009527 |
|
|
fibular aplasia, tibial campomelia, and oligosyndactyly syndrome
|
MONDO_0009526 |
|
|
Bartter disease type 5
|
MONDO_0010503 |
|
|
split hand-foot malformation 3
|
MONDO_0009525 |
|
|
intellectual disability, X-linked 99, syndromic, female-restricted
|
MONDO_0010502 |
|
|
intellectual disability-spasticity-ectrodactyly syndrome
|
MONDO_0009524 |
|
|
intellectual disability-balding-patella luxation-acromicria syndrome
|
MONDO_0010505 |
|
|
Lichtenstein syndrome
|
MONDO_0009523 |
|
|
immunodeficiency 47
|
MONDO_0010504 |
|
|
Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome
|
MONDO_0009522 |
|
|
Xq25 microduplication syndrome
|
MONDO_0010507 |
|
|
leukemia, acute myelocytic, with polyposis coli and colon cancer
|
MONDO_0009521 |
|
|
intellectual disability, X-linked 61
|
MONDO_0010506 |
|
|
3-hydroxy-3-methylglutaric aciduria
|
MONDO_0009520 |
|
|
intellectual disability, X-linked 104
|
MONDO_0010509 |
|
|
intellectual disability, X-linked 103
|
MONDO_0010508 |
|
|
amelogenesis imperfecta type 1E
|
MONDO_0010521 |
|
|
X-linked Alport syndrome
|
MONDO_0010520 |
|
|
X-linked reticulate pigmentary disorder
|
MONDO_0010523 |
|
