|
posterior laryngeal cleft (PLC)
|
C537875 |
|
|
congenital laryngeal clefts
|
C537875 |
|
|
valine metabolism disease
|
37870 |
|
|
Bordetella infectious disease
|
37872 |
|
|
Bordetella caused disease or disorder
|
37872 |
|
|
larsen syndrome, dominant type
|
C537873 |
|
|
laron syndrome due to postreceptor defect
|
C537871 |
|
|
psychomotor retardation, epilepsy, and craniofacial dysmorphism
|
13787 |
|
|
psychomotor retardation, epilepsy, and craniofacial dysmorphism; PMRED
|
http://purl.obolibrary.org/obo/MONDO_0013787 |
|
|
familial, with external and middle ear abnormalities lateral semicircular canal malformation
|
C537879 |
|
|
mixed testicular germ cell cancer of childhood
|
3787 |
|
|
lethal type larsen like syndrome
|
C537872 |
|
|
autosomal dominant larsen syndrome
|
C537873 |
|
