|
GM2 gangliosidosis, B1 variant
|
17728 |
|
|
Tay-Sachs disease, B1 variant
|
17728 |
|
|
acne inversa, familial, 1
|
7728 |
|
|
large-cell lymphoma, anaplastic
|
D017728 |
|
|
large-cell lymphomas, anaplastic
|
D017728 |
|
|
lymphoma, large-cell, anaplastic
|
D017728 |
|
|
hexosaminidase A deficiency, B1 variant
|
17728 |
|
|
NCSTN familial acne inversa
|
7728 |
|
|
acne inversa, familial, 1; ACNINV1
|
http://purl.obolibrary.org/obo/MONDO_0007728 |
|
|
acne inversa, familial, type 1
|
7728 |
|
|
type i oculocutaneous albinism
|
C537728 |
|
|
familial acne inversa caused by mutation in NCSTN
|
7728 |
|
