All terms in MONDO
| Label |
Id |
Description |
|
X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2
|
MONDO_0010522 |
|
|
arthrogryposis spinal muscular atrophy
|
MONDO_0022504 |
|
|
asternia
|
MONDO_0022509 |
|
|
atlanto-axial fusion
|
MONDO_0022510 |
|
|
lymphoblastic leukemia, acute, with lymphomatous features
|
MONDO_0009539 |
|
|
lymphoid system deterioration, progressive
|
MONDO_0009538 |
|
|
obsolete atrial septal defect coronary sinus
|
MONDO_0022512 |
|
|
lymphoid interstitial pneumonia
|
MONDO_0009537 |
|
|
atrophoderma of Pierini and Pasini
|
MONDO_0022513 |
|
|
combined immunodeficiency due to moesin deficiency
|
MONDO_0010514 |
|
|
chronic mucocutaneous candidiasis due to intrinsic defect in lymphoblastic transformation
|
MONDO_0009536 |
|
|
obsolete intellectual disability, X-linked, syndromic, Borck type
|
MONDO_0010513 |
|
|
obsolete lymphedema, congenital recessive
|
MONDO_0009535 |
|
|
midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis
|
MONDO_0010516 |
|
|
Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome
|
MONDO_0010263 |
|
|
chronic mucocutaneous candidiasis due to inhibition of lymphoblastic transformation
|
MONDO_0009534 |
|
|
Meester-Loeys syndrome
|
MONDO_0010515 |
|
|
Dahlberg-Borer-Newcomer syndrome
|
MONDO_0009533 |
|
|
Wiskott-Aldrich syndrome
|
MONDO_0010518 |
|
|
Miller-Dieker lissencephaly syndrome
|
MONDO_0009532 |
|
