|
acute, b- and t-cell lymphocytic leukemia
|
D015456 |
|
|
mental retardation, autosomal recessive 49
|
14567 |
|
|
congenital primary aphakia
|
12456 |
|
|
mental retardation, autosomal recessive 49; MRT49
|
http://purl.obolibrary.org/obo/MONDO_0014567 |
|
|
mental retardation, autosomal recessive type 49
|
14567 |
|
|
iridogoniodysgenesis anomaly, autosomal dominant
|
24456 |
|
|
autosomal dominant axonal Charcot-Marie-Tooth disease type 2U
|
14566 |
|
|
Charcot-Marie-Tooth disease axonal type 2U
|
14566 |
|
|
Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2U
|
14566 |
|
|
Charcot-Marie-Tooth disease, axonal, type 2U
|
14566 |
|
|
Charcot-Marie-Tooth disease, axonal, type 2U; CMT2U
|
http://purl.obolibrary.org/obo/MONDO_0014566 |
|
|
leukemia, mixed, b and t cell
|
D015456 |
|
|
leukemia, mixed, b- and t-cell
|
D015456 |
|
|
apocrine breast carcinoma in situ
|
4562 |
|
