|
nephrotic syndrome 15; NPHS15
|
http://purl.obolibrary.org/obo/MONDO_0033262 |
|
|
nephrotic syndrome 16; NPHS16
|
http://purl.obolibrary.org/obo/MONDO_0033280 |
|
|
CRANIOECTODERMAL dysplasia 2; CED2
|
http://purl.obolibrary.org/obo/MONDO_0013323 |
|
|
Platelet glycoprotein 2B 3A deficiency
|
31332 |
|
|
CRANIOECTODERMAL dysplasia 2
|
13323 |
|
|
cranioectodermal dysplasia 2
|
13323 |
|
|
Diacyclothrombopathia 2B 3A
|
31332 |
|
|
autosomal dominant 7 deafness
|
C563321 |
|
|
SENIOR-Loken syndrome 7; SLSN7
|
http://purl.obolibrary.org/obo/MONDO_0013326 |
|
|
brachydactyly, type A1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and intellectual disability
|
13332 |
|
|
brachydactyly, type A1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and mental retardation
|
13332 |
|
