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1 OMIM reference -
1 associated gene
14 signs/symptoms
PROTEIN INTERACTIONS: 1
16 OMIM references -
4 associated genes
No signs/symptoms info
Alpha-N-acetylgalactosaminidase deficiency type 2
Early-onset autosomal dominant Alzheimer disease

NAGA APP
PSEN1
PSEN2
SORL1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
NAGA
(0.56)
APP



Citations in the biomedical literature:


Alpha-N-acetylgalactosaminidase deficiency type 2
NAGA
Early-onset autosomal dominant Alzheimer disease
APP PSEN1 PSEN2 SORL1



Alpha-N-acetylgalactosaminidase deficiency type 2
Early-onset autosomal dominant Alzheimer disease

Synonym(s):
- Adult-onset Alpha-N-acetylgalactosaminidase deficiency
- Kanzaki disease
- NAGA deficiency type 2
- Schindler disease type 2

Synonym(s):
- EOFAD
- Early-onset familial autosomal dominant Alzheimer disease
- Familial Alzheimer disease

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

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: adulthood
Average age of death: adult
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
No MeSH references
External references:
16 OMIM references -
No MeSH references

Alpha-N-acetylgalactosaminidase deficiency type 2

Very frequent
- Autosomal recessive inheritance
- Hyperkeratosis / ainhum / hyperkeratotic skin fissures
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Telangiectasiae of the skin
- Vascular anomalies of skin / mucosae

Frequent
- Cardiomegaly
- Coarse face
- Corneal clouding / opacity / vascularisation
- Depressed nasal bridge
- Hearing loss / hypoacusia / deafness
- Lymphedema
- Peripheral neuropathy
- Thick lips
- Tinnitus



Early-onset autosomal dominant Alzheimer disease

(no data available)