|
monodermal teratoma (morphologic abnormality)
|
3331 |
|
|
amaurosis fugax (one sided temporary vision loss)
|
43310 |
|
|
Joubert syndrome 31; JBTS31
|
http://purl.obolibrary.org/obo/MONDO_0033310 |
|
|
Joubert syndrome 33; JBTS33
|
http://purl.obolibrary.org/obo/MONDO_0033311 |
|
|
autosomal recessive 37 deafness
|
C564331 |
|
|
Ritscher-Schinzel syndrome 4
|
30331 |
|
|
retinitis pigmentosa 55; RP55
|
http://purl.obolibrary.org/obo/MONDO_0013312 |
|
|
retinitis pigmentosa 56; RP56
|
http://purl.obolibrary.org/obo/MONDO_0013314 |
|
|
retinitis pigmentosa 57; RP57
|
http://purl.obolibrary.org/obo/MONDO_0013315 |
|
|
hemihyperplasia, isolated; IH
|
http://purl.obolibrary.org/obo/MONDO_0009331 |
|
