All terms in MONDO
| Label |
Id |
Description |
|
X-linked lymphoproliferative syndrome
|
MONDO_0010627 |
|
|
obsolete mitochondrial complex II deficiency
|
MONDO_0009641 |
|
|
obsolete mitochondrial complex I deficiency, nuclear type
|
MONDO_0009640 |
|
|
impacted teeth, multiple
|
MONDO_0010629 |
|
|
Strongylida infectious disease, non-human animal
|
MONDO_0700209 |
|
|
helminthiasis, animal
|
MONDO_0025082 |
|
|
Strongylida infectious disease
|
MONDO_0005973 |
|
|
Leber optic atrophy, susceptibility to
|
MONDO_0010640 |
|
|
Leber hereditary optic neuropathy
|
MONDO_0010788 |
|
|
Parvoviridae infectious disease, non-human animal
|
MONDO_0700206 |
|
|
Lesch-Nyhan phenotype with normal HGPRT
|
MONDO_0010642 |
|
|
Lesch-Nyhan syndrome
|
MONDO_0010298 |
|
|
tick-borne infectious disease, non-human animal
|
MONDO_0700201 |
|
|
Anaplasmataceae infectious disease, non-human animal
|
MONDO_0700113 |
|
|
X-linked diffuse leiomyomatosis-Alport syndrome
|
MONDO_0010641 |
|
|
partial deletion of the long arm of chromosome X
|
MONDO_0017007 |
|
|
Caliciviridae infectious disease, non-human animal
|
MONDO_0700208 |
|
|
proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis
|
MONDO_0010644 |
|
|
proteinuria
|
MONDO_0003634 |
|
|
constitutional delay of growth and puberty
|
MONDO_0700207 |
|
