All terms in MONDO
| Label |
Id |
Description |
|
intellectual developmental disorder, autosomal recessive 69
|
MONDO_0032715 |
|
|
leukoencephalopathy, acute reversible, with increased urinary alpha-ketoglutarate
|
MONDO_0032716 |
|
|
lepromatous leprosy
|
MONDO_0005127 |
|
|
facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome
|
MONDO_0032714 |
|
|
tuberculoid leprosy
|
MONDO_0005126 |
|
|
hypertriglyceridemia, familial
|
MONDO_0007788 |
|
|
hypertriglyceridemia
|
MONDO_0005347 |
|
|
combined oxidative phosphorylation deficiency 38
|
MONDO_0032712 |
|
|
hypertrophia musculorum vera
|
MONDO_0007789 |
|
|
obsolete sensory system disease
|
MONDO_0005128 |
|
|
obsolete hypertrichosis lanuginosa congenita
|
MONDO_0007786 |
|
|
obsolete Hibiscus chlorotic ringspot virus infection
|
MONDO_0005123 |
|
|
obsolete cataract, microcephaly, failure to thrive, kyphoscoliosis syndrome
|
MONDO_0020742 |
|
|
Ambras type hypertrichosis universalis congenita
|
MONDO_0007787 |
|
|
pyridoxine-dependent epilepsy caused by ALDH7A1 mutant
|
MONDO_0020741 |
|
|
pyridoxine-dependent epilepsy
|
MONDO_0009945 |
|
|
Pectobacterium carotovorum infection
|
MONDO_0005122 |
|
|
borderline leprosy
|
MONDO_0005125 |
|
|
ectodermal dysplasia and immunodeficiency 1
|
MONDO_0020740 |
|
|
selective pituitary resistance to thyroid hormone
|
MONDO_0007784 |
|
