All terms in MONDO
| Label |
Id |
Description |
|
digital papillary eccrine carcinoma
|
MONDO_0044789 |
|
|
papillary eccrine carcinoma
|
MONDO_0003531 |
|
|
iron overload, susceptibility to
|
MONDO_0859316 |
|
|
Pseudohypoaldosteronism, type IB2, autosomal recessive
|
MONDO_0859317 |
|
|
Pseudohypoaldosteronism, type IB3, autosomal recessive
|
MONDO_0859318 |
|
|
dyskeratosis congenita, autosomal recessive 8
|
MONDO_0859319 |
|
|
neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities
|
MONDO_0859312 |
|
|
neurodevelopmental disorder with speech impairment and with or without seizures
|
MONDO_0859313 |
|
|
developmental and epileptic encephalopathy 108
|
MONDO_0859314 |
|
|
combined hepatocellular carcinoma and cholangiocarcinoma
|
MONDO_0044791 |
|
|
orofaciodigital syndrome 19
|
MONDO_0859310 |
|
|
obsolete congenital melanocytic nevus
|
MONDO_0044790 |
|
|
Charcot-Marie-Tooth disease, demyelinating, type 1J
|
MONDO_0859311 |
|
|
benign melanocytic skin nevus
|
MONDO_0044794 |
|
|
spindle cell nevus
|
MONDO_0044796 |
|
|
large congenital melanocytic nevus
|
MONDO_0044792 |
|
|
epithelioid cell nevus
|
MONDO_0044795 |
|
|
Birt-Hogg-Dube syndrome
|
MONDO_0007607 |
|
|
fibrinolytic defect
|
MONDO_0007605 |
|
|
fibrodysplasia ossificans progressiva
|
MONDO_0007606 |
|
