|
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 |
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leukemia, mixed, b and t cell
|
D015456 |
|
|
leukemia, mixed, b- and t-cell
|
D015456 |
|
|
amelogenesis imperfecta caused by mutation in AMBN
|
14560 |
|
|
apocrine breast carcinoma in situ
|
4562 |
|
|
breast apocrine carcinoma in situ
|
4562 |
|
|
iridogoniodysgenesis caused by mutation in FOXC1
|
24456 |
|
|
3-methylglutaconic aciduria caused by mutation in CLPB
|
14561 |
|
|
nephronophthisis (disease) caused by mutation in NPHP3
|
11456 |
|
|
X-linked, with cerebellar hypoplasia and distinctive facial appearance mental retardation
|
C537456 |
|
|
renal cell carcinoma, Xp11-associated
|
10456 |
|
