All terms in MONDO
| Label |
Id |
Description |
|
Larsen-like osseous dysplasia-short stature syndrome
|
MONDO_0012055 |
|
|
ALG1-congenital disorder of glycosylation
|
MONDO_0012052 |
|
|
aneurysm, intracranial berry, 2
|
MONDO_0012053 |
|
|
nephrolithiasis/osteoporosis, hypophosphatemic
|
MONDO_0000079 |
|
|
acrocephalosyndactyly
|
MONDO_0019796 |
|
|
obsolete nystagmus
|
MONDO_0000077 |
|
|
obsolete myopathy, reducing body, X-linked
|
MONDO_0000072 |
|
|
obsolete myopathy, myofibrillar
|
MONDO_0000071 |
|
|
mycobacterium tuberculosis, susceptibility
|
MONDO_0000070 |
|
|
obsolete neuropathy, hereditary sensory and autonomic
|
MONDO_0000076 |
|
|
obsolete neurodegeneration with brain iron accumulation
|
MONDO_0000074 |
|
|
obsolete nail disorder, nonsyndromic congenital
|
MONDO_0000073 |
|
|
keratoconus 3
|
MONDO_0012069 |
|
|
asthma-related traits, susceptibility to, 2
|
MONDO_0012067 |
|
|
brachial palsy, familial congenital
|
MONDO_0012068 |
|
|
sick sinus syndrome
|
MONDO_0001823 |
|
|
dilated cardiomyopathy 1O
|
MONDO_0012062 |
|
|
autosomal recessive nonsyndromic hearing loss 35
|
MONDO_0012060 |
|
|
obsolete Stevens-Johnson syndrome
|
MONDO_0012065 |
|
|
atrial fibrillation, familial, 1
|
MONDO_0012066 |
|
