All terms in MONDO
| Label |
Id |
Description |
|
obsolete familial partial lipodystrophy
|
MONDO_0000324 |
|
|
obsolete neuromuscular junction disease
|
MONDO_0002983 |
|
|
reticulohistiocytic granuloma
|
MONDO_0002984 |
|
|
obsolete familial adenomatous polyposis
|
MONDO_0000323 |
|
|
mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant
|
MONDO_0014959 |
|
|
Harel-Yoon syndrome
|
MONDO_0014958 |
|
|
language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia
|
MONDO_0014957 |
|
|
obsolete myofibroma
|
MONDO_0002980 |
|
|
spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctate calcifications, and deafness
|
MONDO_0012311 |
|
|
sudden cardiac failure, alcohol-induced
|
MONDO_0014974 |
|
|
sudden cardiac failure, infantile
|
MONDO_0014973 |
|
|
short QT syndrome type 1
|
MONDO_0012312 |
|
|
short QT syndrome
|
MONDO_0000453 |
|
|
chromosome 19q13.11 deletion syndrome, proximal
|
MONDO_0014972 |
|
|
chromosome 19q13.11 deletion syndrome
|
MONDO_0013090 |
|
|
fibrosis of extraocular muscles, congenital, with synergistic divergence
|
MONDO_0012310 |
|
|
amelogenesis imperfecta, hypomaturation type, IIa6
|
MONDO_0014971 |
|
|
obsolete preimplantation embryonic lethality 2
|
MONDO_0014978 |
|
|
distal 10q deletion syndrome
|
MONDO_0012315 |
|
|
partial monosomy of the long arm of chromosome 10
|
MONDO_0016909 |
|
