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Alpha-mannosidosis, infantile form
1 associated gene
2 connected diseases
No signs/symptoms info
Disease Type of connection
Alpha-mannosidosis, adult form
Heritable pulmonary arterial hypertension
Synonym(s):
- Lysosomal alpha-D-mannosidase deficiency, infantile form
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
MAN2B1 O00754609458
No signs/symptoms info available.