|
autosomal recessive nonsyndromic deafness 29
|
13537 |
|
|
autosomal recessive nonsyndromic deafness caused by mutation in CLDN14
|
13537 |
|
|
autosomal recessive nonsyndromic deafness type 29
|
13537 |
|
|
phosphoserine phosphatase deficiency; PSPHD
|
http://purl.obolibrary.org/obo/MONDO_0013531 |
|
|
Bordetella parapertussis disease or disorder
|
1353 |
|
|
atrial fibrillation, familial, 10
|
13530 |
|
|
atrial fibrillation, familial, 10; ATFB10
|
http://purl.obolibrary.org/obo/MONDO_0013530 |
|
|
atrial fibrillation, familial, type 10
|
13530 |
|
|
familial atrial fibrillation caused by mutation in SCN5A
|
13530 |
|
|
wound infections, postoperative
|
D013530 |
|
|
infection due to Bordetella parapertussis
|
1353 |
|
|
deafness, autosomal recessive 29
|
13537 |
|
|
deafness, autosomal recessive 29; DFNB29
|
http://purl.obolibrary.org/obo/MONDO_0013537 |
|
|
CLDN14 autosomal recessive nonsyndromic deafness
|
13537 |
|
|
deafness, autosomal recessive type 29
|
13537 |
|
