All terms in MONDO
| Label |
Id |
Description |
|
juvenile absence epilepsy
|
MONDO_0011876 |
|
|
hypochondroplasia
|
MONDO_0007793 |
|
|
hypogonadotropic hypogonadism 7 with or without anosmia
|
MONDO_0007794 |
|
|
hypogonadotropic hypogonadism 14 with or without anosmia
|
MONDO_0013926 |
|
|
spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3
|
MONDO_0020770 |
|
|
familial hypocalciuric hypercalcemia 1
|
MONDO_0007791 |
|
|
familial hypocalciuric hypercalcemia 2
|
MONDO_0007792 |
|
|
obsolete autosomal ichthyosis syndrome with other associated signs
|
MONDO_0029102 |
|
|
epilepsy, childhood absence, susceptibility to, 1
|
MONDO_0020759 |
|
|
obsolete MONDO:0020758
|
MONDO_0020758 |
|
|
X-linked external auditory canal atresia-dilated internal auditory canal-facial dysmorphism syndrome
|
MONDO_0044702 |
|
|
sporadic hemiplegic migraine
|
MONDO_0020757 |
|
|
childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder
|
MONDO_0044701 |
|
|
migraine, familial hemiplegic, 1
|
MONDO_0020756 |
|
|
cytophagic histiocytic panniculitis
|
MONDO_0019789 |
|
|
oropharyngeal carcinoma
|
MONDO_0044926 |
|
|
obsolete heart block
|
MONDO_0020755 |
|
|
inherited cardiac tumor
|
MONDO_0017129 |
|
|
encephalopathy, acute, infection-induced, susceptibility to, 9
|
MONDO_0032742 |
|
|
severe intellectual disability-epilepsy-anal anomalies-distal phalangeal hypoplasia
|
MONDO_0019786 |
|
