neurogenic scapuloperoneal syndrome, Kaeser type
human disease
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neurogenic scapuloperoneal syndrome, Kaeser type
Summary
neurogenic scapuloperoneal syndrome, Kaeser type is a hereditary disorder[1].
Key Facts
- neurogenic scapuloperoneal syndrome, Kaeser type's instance of is recorded as hereditary disorder[2].
- neurogenic scapuloperoneal syndrome, Kaeser type's instance of is recorded as rare disease[3].
- neurogenic scapuloperoneal syndrome, Kaeser type's instance of is recorded as class of disease[4].
- neurogenic scapuloperoneal syndrome, Kaeser type is a type of qualitative or quantitative defects of desmin[5].
- neurogenic scapuloperoneal syndrome, Kaeser type is a type of genetic motor neuron disease[6].
- neurogenic scapuloperoneal syndrome, Kaeser type is a type of autosomal dominant disease[7].
- neurogenic scapuloperoneal syndrome, Kaeser type is a type of muscular disease[8].
- neurogenic scapuloperoneal syndrome, Kaeser type's genetic association is recorded as DES[9].
- neurogenic scapuloperoneal syndrome, Kaeser type's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_85146[10].
- neurogenic scapuloperoneal syndrome, Kaeser type's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111551[11].
- neurogenic scapuloperoneal syndrome, Kaeser type's exact match is recorded as http://identifiers.org/doid/DOID:0111551[12].