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Congenital sialidosis type 2

1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Galactosialidosis

1 OMIM reference -
1 associated gene
10 signs/symptoms

Congenital sialidosis type 2

Galactosialidosis

(UniProt - OMIM)

(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	NEU1	(0.92)	CTSA

Citations in the biomedical literature:

Congenital sialidosis type 2		Galactosialidosis
	Synonym(s): (no synonyms)		Synonym(s): - Goldberg syndrome - Neuraminidase deficiency with beta-galactosidase deficiency

	Classification (Orphanet): - Inborn errors of metabolism - Rare bone disease - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease - Rare neurologic disease - Rare renal disease		Classification (Orphanet): - Inborn errors of metabolism - Rare bone disease - Rare eye disease - Rare genetic disease - Rare neurologic disease

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

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: - Type of inheritance: autosomal recessive

	External references: No OMIM references No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C536411

Galactosialidosis
	Very frequent - Anomalies of spine, vertebrae and pelvis - Autosomal recessive inheritance - Coarse face - Corneal clouding / opacity / vascularisation - Dysostosis / chondrodysplasia / osteodysplasia / osteochondrosis / skeletal dysplasia - Hearing loss / hypoacusia / deafness - Intellectual deficit / mental / psychomotor retardation / learning disability - Macular pigmentary anomaly / cherry-red spot - Seizures / epilepsy / absences / spasms / status epilepticus - Short stature / dwarfism / nanism
Congenital sialidosis type 2
(no data available)