ODCs

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4 OMIM references -
1 associated gene
2 signs/symptoms

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Hereditary gingival fibromatosis

Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SOS1	(0.84)	CSF1R

Citations in the biomedical literature:

Hereditary gingival fibromatosis		Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
	Synonym(s): - Autosomal dominant gingival fibromatosis - Autosomal dominant gingival hyperplasia - Hereditary gingival hyperplasia		Synonym(s): - ALSP - Autosomal dominant leukoencephalopathy with neuroaxonal spheroids - HDLS - Hereditary diffuse leukoencephalopathy with spheroids - POLD - Pigmentary orthochromatic leukodystrophy

	Classification (Orphanet): - Rare genetic disease - Rare odontologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Diseases of the digestive system -		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: adult Type of inheritance: autosomal dominant

	External references: 4 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

Hereditary gingival fibromatosis
	Very frequent - Autosomal dominant inheritance - Thickened / hypertrophic / fibromatous gingivae
Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
(no data available)