All terms in MONDO
| Label | Id | Description |
|---|---|---|
| cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1 | MONDO_0000914 | |
| balloon cell malignant melanoma | MONDO_0000929 | |
| cutaneous melanoma | MONDO_0005012 | |
| age-related hearing impairment 1 | MONDO_0012910 | |
| age-related hearing impairment | MONDO_0005562 | |
| compensatory emphysema | MONDO_0000924 | |
| interstitial emphysema | MONDO_0000923 | |
| eyelid melanoma | MONDO_0000928 | |
| eyelid cancer | MONDO_0021313 | |
| asymptomatic neurosyphilis | MONDO_0000927 | |
| eye accommodation disease | MONDO_0000926 | |
| hyperlucent lung | MONDO_0000925 | |
| complement component 6 deficiency | MONDO_0012908 | |
| skeletal defects, genital hypoplasia, and intellectual disability | MONDO_0012909 | |
| nodular malignant melanoma | MONDO_0000930 | |
| autosomal dominant nonsyndromic hearing loss 27 | MONDO_0012902 | |
| autosomal recessive nonsyndromic hearing loss 45 | MONDO_0012903 | |
| cardiomyopathy, familial restrictive, 3 | MONDO_0012900 | |
| inherited prekallikrein deficiency | MONDO_0012901 | |
| prekallikrein deficiency | MONDO_0044744 |