neuronal ceroid lipofuscinosis 10 (Q32140575)
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neuronal ceroid lipofuscinosis that has material basis in homozygous or compound heterozygous mutation in the CTSD gene on chromosome 11p15
- neuronal ceroid lipofuscinosis cathepsin D-deficient
- CLN10
- neuronal ceroid lipofuscinosis due to cathepsin D deficiency
- Cathepsin D deficiency
- CEROID LIPOFUSCINOSIS, NEURONAL, 10
- neuronal ceroid lipofuscinosis type 10
- CLN10 disease, juvenile (subtype)
- CEROID LIPOFUSCINOSIS, NEURONAL, 10; CLN10
- Ceroid lipofuscinosis neuronal Cathepsin D-deficient
- Ceroid Lipofuscinosis, Neuronal, type 10
- Ceroid Lipofuscinosis, Neuronal, Cathepsin D-Deficient
- Neuronal Ceroid Lipofuscinosis, Congenital
- CLN10 disease, congenital (subtype)
- CLN10 disease, adult (subtype)
- CLN10 disease, late infantile (subtype)
- CLN10 disease
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | neuronal ceroid lipofuscinosis 10 |
neuronal ceroid lipofuscinosis that has material basis in homozygous or compound heterozygous mutation in the CTSD gene on chromosome 11p15 |
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