|
pituitary hormone deficiency, combined, type 3
|
9091 |
|
|
pituitary hormone deficiency, combined, with rigid cervical spine
|
9091 |
|
|
leukoencephalopathy, hereditary diffuse, with spheroids
|
9096 |
|
|
leukoencephalopathy, hereditary diffuse, with spheroids; HDLS
|
http://purl.obolibrary.org/obo/MONDO_0009096 |
|
|
MPZ Charcot-Marie-Tooth disease
|
11909 |
|
|
Pestivirus caused disease or disorder
|
5909 |
|
|
Pestivirus infectious disease
|
5909 |
|
|
pestivirus infectious disease
|
5909 |
|
|
primary ciliary dyskinesia 34
|
14909 |
|
|
cataract, autosomal dominant, multiple types 1
|
C566909 |
|
|
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 |
|
|
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 |
|
