|
rare hemorrhagic disorder due to a constitutional thrombopathy and/or thrombocytopenia
|
http://purl.obolibrary.org/obo/MONDO_0019097 |
|
|
Charcot-Marie-Tooth disease, dominant intermediate D
|
11909 |
|
|
Charcot-Marie-Tooth neuropathy dominant intermediate D
|
11909 |
|
|
Charcot-Marie-Tooth disease, dominant intermediate D; CMTDID
|
http://purl.obolibrary.org/obo/MONDO_0011909 |
|
|
Charcot-Marie-Tooth disease dominant intermediate d
|
11909.0 |
|
|
primary ciliary dyskinesia 34
|
14909 |
|
|
primary ciliary dyskinesia 34 without situs inversus
|
14909 |
|
|
Charcot-Marie-Tooth disease dominant intermediate type D
|
11909 |
|
|
BCG infection, generalized familial semibenign, autosomal dominant
|
C565909 |
|
|
primary ciliary dyskinesia caused by mutation in DNAJB13
|
14909 |
|
|
primary ciliary dyskinesia type 34
|
14909 |
|
|
van den ende gupta syndrome
|
C535909 |
|
|
van den ende-gupta syndrome
|
C535909 |
|
|
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 |
|
