All terms in MONDO
| Label |
Id |
Description |
|
congenital high-molecular-weight kininogen deficiency
|
MONDO_0009234 |
|
|
Fibulo-ulnar hypoplasia-renal anomalies syndrome
|
MONDO_0009233 |
|
|
Fuhrmann syndrome
|
MONDO_0009232 |
|
|
brittle cornea syndrome
|
MONDO_0009242 |
|
|
osteoarthritis susceptibility 6
|
MONDO_0012894 |
|
|
intellectual disability, X-linked 20
|
MONDO_0010231 |
|
|
fountain syndrome
|
MONDO_0009241 |
|
|
intellectual disability, X-linked 23
|
MONDO_0010230 |
|
|
torsion dystonia 17
|
MONDO_0012895 |
|
|
formiminoglutamic aciduria
|
MONDO_0009240 |
|
|
bone fragility with contractures, arterial rupture, and deafness
|
MONDO_0012892 |
|
|
heterotopia, periventricular, X-linked dominant
|
MONDO_0010233 |
|
|
osteoarthritis susceptibility 5
|
MONDO_0012893 |
|
|
intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked
|
MONDO_0010232 |
|
|
narcolepsy 4, susceptibility to
|
MONDO_0012898 |
|
|
X-linked intellectual disability-psychosis-macroorchidism syndrome
|
MONDO_0010235 |
|
|
alopecia, androgenetic, 3
|
MONDO_0012899 |
|
|
obsolete body length, mouse, human homolog
|
MONDO_0010234 |
|
|
X-linked intellectual disability-plagiocephaly syndrome
|
MONDO_0010237 |
|
|
psoriasis 10, susceptibility to
|
MONDO_0012896 |
|
