|
nephrotic syndrome 15; NPHS15
|
http://purl.obolibrary.org/obo/MONDO_0033262 |
|
|
nephrotic syndrome 16; NPHS16
|
http://purl.obolibrary.org/obo/MONDO_0033280 |
|
|
Glanzmann thrombasthenia 1
|
31332 |
|
|
transient neonatal, 1 diabetes mellitus
|
C563322 |
|
|
Platelet glycoprotein 2B 3A deficiency
|
31332 |
|
|
autosomal recessive 12 deafness
|
C563327 |
|
|
cerebrospinal fluid Drainages
|
43327 |
|
|
autosomal dominant 7 deafness
|
C563321 |
|
|
CRANIOECTODERMAL dysplasia 2
|
13323 |
|
|
cranioectodermal dysplasia 2
|
13323 |
|
|
FORSYTHE-WAKELING syndrome; FWS
|
http://purl.obolibrary.org/obo/MONDO_0013321 |
|
|
SENIOR-Loken syndrome 7; SLSN7
|
http://purl.obolibrary.org/obo/MONDO_0013326 |
|
