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CLN10 disease
1 OMIM reference -
1 associated gene
32 connected diseases
No signs/symptoms info
Disease Type of connection
Atypical Gaucher disease due to saposin C deficiency
Encephalopathy due to prosaposin deficiency
Infantile Krabbe disease
Metachromatic leukodystrophy, adult form
Metachromatic leukodystrophy, juvenile form
Metachromatic leukodystrophy, late infantile form
Early-onset autosomal dominant Alzheimer disease
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16
Autosomal dominant methemoglobinemia
Hb Bart's hydrops fetalis
Hemoglobin H disease
Autosomal recessive distal renal tubular acidosis with deafness
Dedifferentiated liposarcoma
Distal 22q11.2 microdeletion syndrome
Estrogen resistance syndrome
LIG4 syndrome
Omenn syndrome
Spondylometaphyseal dysplasia - cone-rod dystrophy
Well-differentiated liposarcoma
Galactosialidosis
MODY syndrome
Permanent neonatal diabetes mellitus
Familial thyroid dyshormonogenesis
Fibronectin glomerulopathy
Hereditary cerebral hemorrhage with amyloidosis, Icelandic type
Unverricht-Lundborg disease
Synonym(s):
- Cathepsin D deficiency

Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

Epidemiological data:
Class of prevalence: -
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references

Gene symbol UniProt reference OMIM reference
CTSD P07339116840
No signs/symptoms info available.