|
Hermansky-Pudlak syndrome 2
|
11997 |
|
|
myeloid leukemia, chronic
|
11996 |
|
|
disease of anatomical entity
|
http://purl.obolibrary.org/obo/MONDO_0021199 |
|
|
disease by anatomical system
|
21199.0 |
|
|
disease of anatomical system
|
http://purl.obolibrary.org/obo/MONDO_0021199 |
|
|
disorder of anatomical system
|
http://purl.obolibrary.org/obo/MONDO_0021199 |
|
|
Platelet defects and oculocutaneous albinism
|
11997 |
|
|
Hermansky-Pudlak syndrome caused by mutation in AP3B1
|
11997 |
|
|
hematopoeitic - chronic myelocytic leukemia (CML)
|
11996 |
|
|
BCR-ABL Positive chronic myelogenous leukemia
|
11996 |
|
|
CML - chronic myelogenous leukemia
|
11996 |
|
|
P2RX2 autosomal dominant nonsyndromic deafness
|
11994 |
|
|
autosomal recessive deafness 38
|
11991 |
|
|
autosomal dominant deafness 41
|
11994 |
|
