All terms in MONDO
| Label |
Id |
Description |
|
Treacher Collins syndrome 2
|
MONDO_0013385 |
|
|
autosomal recessive nonsyndromic hearing loss 74
|
MONDO_0013386 |
|
|
Hirschsprung disease, susceptibility to, 3
|
MONDO_0013383 |
|
|
Hirschsprung disease, susceptibility to, 4
|
MONDO_0013384 |
|
|
azoospermia, obstructive, with nephrolithiasis
|
MONDO_0025356 |
|
|
multiple congenital anomalies-neurodevelopmental syndrome, X-linked
|
MONDO_0025351 |
|
|
spermatogenic failure, X-linked, 3
|
MONDO_0025354 |
|
|
developmental and epileptic encephalopathy, 90
|
MONDO_0025353 |
|
|
acne inversa, familial, 3
|
MONDO_0013398 |
|
|
obsolete cardiomyopathy, dilated, 1T
|
MONDO_0013399 |
|
|
autosomal recessive spinocerebellar ataxia 10
|
MONDO_0013392 |
|
|
distal 7q11.23 microdeletion syndrome
|
MONDO_0013393 |
|
|
autosomal recessive limb-girdle muscular dystrophy type 2Q
|
MONDO_0013390 |
|
|
sterol carrier protein 2 deficiency
|
MONDO_0013391 |
|
|
chromosome 1p32-p31 deletion syndrome
|
MONDO_0013396 |
|
|
acne inversa, familial, 2
|
MONDO_0013397 |
|
|
porencephaly-microcephaly-bilateral congenital cataract syndrome
|
MONDO_0013394 |
|
|
retinitis pigmentosa 4
|
MONDO_0013395 |
|
|
brucellosis, bovine
|
MONDO_0025389 |
|
|
avian leukosis
|
MONDO_0025381 |
|
