|
wolcott-rallison syndrome
|
C536739 |
|
|
Wolfram-like syndrome, autosomal dominant
|
13673 |
|
|
WOLFRAM-like syndrome, autosomal dominant
|
http://purl.obolibrary.org/obo/MONDO_0013673 |
|
|
WOLFRAM-like syndrome, autosomal dominant; WFSL
|
http://purl.obolibrary.org/obo/MONDO_0013673 |
|
|
multiple, with early-onset diabetes mellitus epiphyseal dysplasia
|
C536739 |
|
|
asymmetric, with polysyndactyly and abnormal skin and gut development craniofacial malformations
|
C536735 |
|
|
chromosome xq duplication syndrome
|
C536732 |
|
|
apical myocardial infarction
|
3673 |
|
|
x chromosome, trisomy xpter xq13
|
C536731 |
|
|
x chromosome, trisomy xq25
|
C536733 |
|
|
hearing loss, progressive, with optic atrophy and/or impaired glucose Regulation
|
13673 |
|
