All terms in MONDO
| Label |
Id |
Description |
|
congenital disorder of glycosylation, type IIr
|
MONDO_0026765 |
|
|
obsolete episodic pain syndrome, familial
|
MONDO_0000157 |
|
|
holoprosencephaly 13, X-linked
|
MONDO_0026763 |
|
|
obsolete Trichohepatoenteric syndrome
|
MONDO_0000154 |
|
|
immunodeficiency 74, COVID-19-related, X-linked
|
MONDO_0026767 |
|
|
obsolete warfarin sensitivity, X-linked
|
MONDO_0026768 |
|
|
developmental dysplasia of the hip
|
MONDO_0000158 |
|
|
Wieacker-Wolff syndrome, female-restricted
|
MONDO_0026762 |
|
|
Wieacker-Wolff syndrome (spectrum)
|
MONDO_0025445 |
|
|
thiamine-responsive dysfunction syndrome
|
MONDO_0000152 |
|
|
disorder of thiamine metabolism and transport
|
MONDO_0017578 |
|
|
obsolete spondylometaphyseal dysplasia
|
MONDO_0000150 |
|
|
familial hemophagocytic lymphohistiocytosis 3
|
MONDO_0012146 |
|
|
coronary heart disease, susceptibility to, 5
|
MONDO_0012147 |
|
|
Waardenburg syndrome type 2D
|
MONDO_0012144 |
|
|
macular degeneration, age-related, 3
|
MONDO_0012145 |
|
|
obsolete drug metabolism, poor, CYP2D6-related
|
MONDO_0012148 |
|
|
attention deficit-hyperactivity disorder, susceptibility to, 1
|
MONDO_0012149 |
|
|
orofacial cleft 5
|
MONDO_0012142 |
|
|
cleft lip and alveolus
|
MONDO_0015420 |
|
