All terms in MONDO
| Label |
Id |
Description |
|
intellectual disability, FRA12A type
|
MONDO_0007634 |
|
|
Frasier syndrome
|
MONDO_0007635 |
|
|
intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies
|
MONDO_0859080 |
|
|
obsolete fragile site, Distamycin a type, rare, fra(16)(q22.1)
|
MONDO_0007632 |
|
|
obsolete blood group, diego system
|
MONDO_0020610 |
|
|
chromosome Xq13 duplication syndrome
|
MONDO_0859081 |
|
|
Friedreich ataxia, so-called, with optic atrophy and sensorineural deafness
|
MONDO_0007633 |
|
|
North Carolina macular dystrophy
|
MONDO_0007630 |
|
|
systemic lupus erythematosus 17
|
MONDO_0859083 |
|
|
chromosome 16p12.1 deletion syndrome, 520kb
|
MONDO_0007631 |
|
|
Rieger anomaly
|
MONDO_0019628 |
|
|
isolated congenital alacrima
|
MONDO_0019627 |
|
|
isolated ankyloblepharon filiforme adnatum
|
MONDO_0019626 |
|
|
eyelid border anomaly
|
MONDO_0020155 |
|
|
chronic pneumonitis of infancy
|
MONDO_0019621 |
|
|
congenital esophageal diverticulum
|
MONDO_0019620 |
|
|
non-specific interstitial pneumonia
|
MONDO_0019622 |
|
|
obsolete gastric juice peptides
|
MONDO_0007649 |
|
|
gastric volvulus, intrathoracic
|
MONDO_0007647 |
|
|
hereditary diffuse gastric adenocarcinoma
|
MONDO_0007648 |
|
