|
juvenile amyotrophic lateral sclerosis 4
|
C566550 |
|
|
Wilson Turner intellectual disability syndrome (formerly)
|
10665 |
|
|
pseudohermaphroditism, male internal
|
C536665 |
|
|
autosomal dominant lewy body parkinson disease 3
|
C566552 |
|
|
muscular dystrophy, limb-girdle, type 1e
|
C566589 |
|
|
familial pancreatic lymphoma
|
C566516 |
|
|
muscular dystrophy, limb-girdle, type 2g
|
C566599 |
|
|
classical Hodgkin lymphoma, nodular sclerosis
|
4665 |
|
|
high grade malignant neoplasm
|
20665 |
|
|
late-onset biotin-responsive multiple carboxylase deficiency
|
9665 |
|
|
macrotia, and mental retardation microcephaly
|
C566525 |
|
|
Wilson-TURNER X-linked mental retardation syndrome
|
10665 |
|
|
Wilson Turner mental retardation syndrome (formerly)
|
10665 |
|
|
Wilson-TURNER X-linked mental retardation syndrome; WTS
|
http://purl.obolibrary.org/obo/MONDO_0010665 |
|
