All terms in MONDO
| Label |
Id |
Description |
|
upper limb defect-eye and ear abnormalities syndrome
|
MONDO_0010125 |
|
|
dystonia 16
|
MONDO_0012789 |
|
|
thumb, distal hyperextensibility of
|
MONDO_0010124 |
|
|
thymoma, familial
|
MONDO_0010127 |
|
|
juvenile cataract-microcornea-renal glucosuria syndrome
|
MONDO_0012786 |
|
|
thymic aplasia with fetal death
|
MONDO_0010126 |
|
|
obsolete catatrichy
|
MONDO_0022109 |
|
|
celiac disease, susceptibility to, 11
|
MONDO_0012780 |
|
|
celiac disease, susceptibility to, 12
|
MONDO_0012781 |
|
|
spermatogenic failure, X-linked, 4
|
MONDO_0024773 |
|
|
intellectual developmental disorder, X-linked, syndromic, Pilorge type
|
MONDO_0024772 |
|
|
central centrifugal cicatricial alopecia
|
MONDO_0022113 |
|
|
immunodeficiency 98 with autoinflammation, X-linked
|
MONDO_0024777 |
|
|
inherited threoninemia
|
MONDO_0010118 |
|
|
3M syndrome 1
|
MONDO_0010117 |
|
|
3-M syndrome
|
MONDO_0007477 |
|
|
dyssegmental dysplasia, Rolland-Desbuquois type
|
MONDO_0009139 |
|
|
perlecan-related bone disorder
|
MONDO_0019689 |
|
|
celiac disease, susceptibility to, 10
|
MONDO_0012779 |
|
|
dysosteosclerosis
|
MONDO_0009138 |
|
