|
retinal nonattachment and falciform detachment
|
9097 |
|
|
rare bleeding disorder due to a constitutional platelet anomaly
|
http://purl.obolibrary.org/obo/MONDO_0019097 |
|
|
rare hemorrhagic disorder due to a constitutional platelet anomaly
|
http://purl.obolibrary.org/obo/MONDO_0019097 |
|
|
rare bleeding disorder due to a constitutional thrombopathy and/or thrombocytopenia
|
http://purl.obolibrary.org/obo/MONDO_0019097 |
|
|
rare hemorrhagic disorder due to a constitutional thrombopathy and/or thrombocytopenia
|
http://purl.obolibrary.org/obo/MONDO_0019097 |
|
|
hemorrhagic disorder due to a constitutional platelet anomaly
|
19097.0 |
|
|
rare coagulopathy due to a constitutional platelet anomaly
|
http://purl.obolibrary.org/obo/MONDO_0019097 |
|
|
rare coagulopathy due to a constitutional thrombopathy and/or thrombocytopenia
|
http://purl.obolibrary.org/obo/MONDO_0019097 |
|
|
retinal nonattachment, nonsyndromic congenital
|
9097 |
|
|
autosomal recessive persistent hyperplastic primary vitreous
|
9097 |
|
|
persistent hyperplastic primary vitreous, autosomal recessive
|
9097 |
|
|
persistent hyperplastic primary vitreous, autosomal recessive; PHPVAR
|
http://purl.obolibrary.org/obo/MONDO_0009097 |
|
|
persistent fetal vasculature
|
9097 |
|
