All terms in MONDO
| Label |
Id |
Description |
|
hidrotic ectodermal dysplasia, Christianson-Fourie type
|
MONDO_0011063 |
|
|
aprosencephaly cerebellar dysgenesis
|
MONDO_0011062 |
|
|
Hunter-McAlpine craniosynostosis
|
MONDO_0011065 |
|
|
primary orthostatic disorder
|
MONDO_0035014 |
|
|
lethal chondrodysplasia, Seller type
|
MONDO_0011064 |
|
|
obsolete genetic primary orthostatic disorder
|
MONDO_0035013 |
|
|
Eagle syndrome
|
MONDO_0023035 |
|
|
Coffin-Siris syndrome 12
|
MONDO_0025699 |
|
|
obsolete elongated styloid process syndrome
|
MONDO_0023037 |
|
|
eccentrochondrodysplasia
|
MONDO_0023038 |
|
|
eccrine mucinous carcinoma
|
MONDO_0023039 |
|
|
dystonia 30
|
MONDO_0025691 |
|
|
microcephaly, epilepsy, and diabetes syndrome 2
|
MONDO_0025690 |
|
|
dysmorphism cleft palate loose skin
|
MONDO_0023030 |
|
|
obsolete dysostosis acral with facial and genital abnormalities
|
MONDO_0023031 |
|
|
MONDO_0023033
|
MONDO_0023033 |
|
|
anterior chamber cleavage disorder, cerebellar hypoplasia, hypothyroidism, and tracheal stenosis
|
MONDO_0011078 |
|
|
microcephaly, corpus callosum dysgenesis, and cleft lip/palate
|
MONDO_0011077 |
|
|
rhizomelic dysplasia, Patterson-Lowry type
|
MONDO_0011079 |
|
|
van Maldergem syndrome 1
|
MONDO_0011070 |
|
