ODCs

Cytoscape Web

Click node...

1 OMIM reference -
1 associated gene
12 signs/symptoms

PROTEIN INTERACTIONS: 1

Inherited Creutzfeldt-Jakob disease

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

MASA syndrome

Inherited Creutzfeldt-Jakob disease

(UniProt - OMIM)

(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	L1CAM	(0.59)	PRNP

Citations in the biomedical literature:

MASA syndrome		Inherited Creutzfeldt-Jakob disease
	Synonym(s): - Intellectual defici-aphasia-shuffling gait-adducted thumbs syndrome		Synonym(s): - Inherited CJD

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Certain infectious and parasitic diseases -

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: no data available Type of inheritance: x-linked recessive		Epidemiological data: (no data available)

	External references: 1 OMIM reference - 1 MeSH reference: C536029		External references: 1 OMIM reference - No MeSH references

MASA syndrome
	Very frequent - Abnormal gait - Clasp thumb / thumb adduction / distal thumb phalangeal bone deviated / large - Hemiplegia / diplegia / hemiparesia / limb palsy - Hypereflexia - Intellectual deficit / mental / psychomotor retardation / learning disability - Short stature / dwarfism / nanism - Speech troubles / aphasia / dysphasia / echolalia / mutism / logorrhea / dysprosodia - X-linked recessive inheritance Frequent - Camptodactyly of fingers - Clinodactyly of fifth finger Occasional - Corpus callosum / septum pellucidum total / partial agenesis - Dilated cerebral ventricles without hydrocephaly
Inherited Creutzfeldt-Jakob disease
(no data available)