All terms in MONDO
| Label |
Id |
Description |
|
rheumatoid arthritis
|
MONDO_0008383 |
|
|
post-traumatic epilepsy
|
MONDO_0043264 |
|
|
epilepsy
|
MONDO_0005027 |
|
|
pregnancy loss, recurrent, 4
|
MONDO_0800310 |
|
|
infertility disorder
|
MONDO_0005047 |
|
|
vas deferens, congenital unilateral aplasia of
|
MONDO_0800311 |
|
|
congenital bilateral absence of vas deferens
|
MONDO_0018801 |
|
|
xeroderma pigmentosum, type G/cockayne syndrome
|
MONDO_0800314 |
|
|
xeroderma pigmentosum-Cockayne syndrome complex
|
MONDO_0016354 |
|
|
woolly hair, autosomal recessive 1, with or without hypotrichosis
|
MONDO_0800312 |
|
|
isolated familial woolly hair disorder
|
MONDO_0008686 |
|
|
xeroderma pigmentosum, type F/cockayne syndrome
|
MONDO_0800313 |
|
|
Emery-Deifuss muscular dystrophy 6, X-linked
|
MONDO_0800318 |
|
|
Emery-Dreifuss muscular dystrophy
|
MONDO_0016830 |
|
|
cone dystrophy 5, X-linked
|
MONDO_0800319 |
|
|
retinal degeneration
|
MONDO_0004580 |
|
|
obsolete contiguous ABCD1/DXS1375E deletion syndrome
|
MONDO_0800316 |
|
|
premature ovarian failure 4
|
MONDO_0800317 |
|
|
black locks with albinism and deafness syndrome
|
MONDO_0800300 |
|
|
obsolete hypophosphatasia, perinatal lethal
|
MONDO_0800303 |
|
