All terms in MONDO
| Label |
Id |
Description |
|
enolase, sperm specific
|
MONDO_0007543 |
|
|
multiple endocrine neoplasia type 1
|
MONDO_0007540 |
|
|
endometriosis, susceptibility to, 1
|
MONDO_0007541 |
|
|
ectopic Cushing syndrome
|
MONDO_0020527 |
|
|
hemoglobin D disease
|
MONDO_0019537 |
|
|
acute megakaryoblastic leukemia in down syndrome
|
MONDO_0020526 |
|
|
typical hemolytic-uremic syndrome
|
MONDO_0019536 |
|
|
obsolete retinopathy of prematurity
|
MONDO_0019539 |
|
|
primary parathyroid hyperplasia
|
MONDO_0020524 |
|
|
Gaisbock syndrome
|
MONDO_0019538 |
|
|
familial parathyroid adenoma
|
MONDO_0020523 |
|
|
paroxysmal cold hemoglobinuria
|
MONDO_0019533 |
|
|
autoimmune hemolytic anemia, warm type
|
MONDO_0019532 |
|
|
drug-induced autoimmune hemolytic anemia
|
MONDO_0019535 |
|
|
mixed-type autoimmune hemolytic anemia
|
MONDO_0019534 |
|
|
White-Kernohan syndrome
|
MONDO_0859169 |
|
|
hemolytic anemia due to glutathione reductase deficiency
|
MONDO_0019531 |
|
|
neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities
|
MONDO_0859165 |
|
|
myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy
|
MONDO_0859168 |
|
|
onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome
|
MONDO_0859161 |
|
