|
Charcot Marie Tooth disease dominant intermediate 3
|
11909 |
|
|
obsolete aplasia cutis congenita recessive
|
21909.0 |
|
|
Charcot-Marie-Tooth disease caused by mutation in MPZ
|
11909 |
|
|
obsolete meconium aspiration syndrome
|
19090.0 |
|
|
Charcot-Marie-Tooth neuropathy, dominant Intermediate D
|
11909 |
|
|
specific antibody deficiency
|
19093 |
|
|
MPZ Charcot-Marie-Tooth disease
|
11909 |
|
|
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 |
|
|
Charcot-Marie-Tooth disease, dominant Intermediate type D
|
11909 |
|
|
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 |
|
|
Charcot-Marie-Tooth disease dominant intermediate D
|
11909 |
|
