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Intellectual deficiency - hypotonia - spasticity - sleep disorder
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Oculootodental syndrome
1 OMIM reference -
2 associated genes
No signs/symptoms info
Intellectual deficiency - hypotonia - spasticity - sleep disorder
Oculootodental syndrome

ANK3
(UniProt - OMIM)
 FADD
(UniProt - OMIM)
FGF3
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ANK3
(0.55)
FADD


Citations in the biomedical literature:


Intellectual deficiency - hypotonia - spasticity - sleep disorder
ANK3
Oculootodental syndrome
FADD FGF3



Intellectual deficiency - hypotonia - spasticity - sleep disorder
Oculootodental syndrome

Synonym(s):
(no synonyms)

Synonym(s):
- OOD
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare odontologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the digestive system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.