: Human diseases: Walker-Warburg syndrome

... > nervous system diseases > neurological disorder > psychomotor disorder > psychomotor retardation > Walker-Warburg syndrome

... > nervous system diseases > central nervous system diseases > cerebral disorder > hydrocephaly > Walker-Warburg syndrome

disease > congenital disease > malformation > retinal dysplasia > Walker-Warburg syndrome

disease > dysplasia > retinal dysplasia > Walker-Warburg syndrome

disease > genetic disease > hereditary disease > retinal dysplasia > Walker-Warburg syndrome

disease > eye disease > retinopathy > retinal dysplasia > Walker-Warburg syndrome

disease > symptom > muscle tonus alteration > hypotonia > Walker-Warburg syndrome

disease > striated muscle disease > muscle tonus alteration > hypotonia > Walker-Warburg syndrome

... > nervous system diseases > neurological disorder > muscle tonus alteration > hypotonia > Walker-Warburg syndrome

disease > genetic disease > hereditary disease > muscular dystrophy > Walker-Warburg syndrome

disease > nervous system diseases > neuromuscular diseases > muscular dystrophy > Walker-Warburg syndrome

disease > degenerative disease > dystrophy > muscular dystrophy > Walker-Warburg syndrome

disease > congenital disease > malformation > lissencephaly > Walker-Warburg syndrome

... > nervous system diseases > central nervous system diseases > cerebral disorder > lissencephaly > Walker-Warburg syndrome

Walker-Warburg syndrome

Walker–Warburg syndrome (WWS), also called Warburg syndrome, Chemke syndrome, HARD syndrome (Hydrocephalus, Agyria and Retinal Dysplasia), Pagon syndrome, cerebroocular dysgenesis (COD) or cerebroocular dysplasia-muscular dystrophy syndrome (COD-MD), is a rare form of autosomal recessive congenital muscular dystrophy. (Wikipedia)

http://data.loterre.fr/ark:/67375/VH8-GFD1FH34-L

RDF/XML TURTLE JSON-LD

Loterre