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13 OMIM references -
14 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
6 signs/symptoms
Autosomal dominant nonsyndromic intellectual deficit
Dental ankylosis

CACNG2 PTH1R
CDH15
CTNNB1
DOCK8
DYNC1H1
DYRK1A
EPB41L1
GRIN1
GRIN2B
KIF1A
KIRREL3
MBD5
SYNGAP1
TCF4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CTNNB1
(0.65)
PTH1R



Citations in the biomedical literature:


Autosomal dominant nonsyndromic intellectual deficit
CACNG2 CDH15 CTNNB1 DOCK8 DYNC1H1 DYRK1A
EPB41L1 GRIN1 GRIN2B KIF1A KIRREL3 MBD5
SYNGAP1 TCF4
Dental ankylosis
PTH1R



Autosomal dominant nonsyndromic intellectual deficit
Dental ankylosis

Synonym(s):
(no synonyms)

Synonym(s):
- Ankylosis of teeth

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

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

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

External references:
13 OMIM references -
No MeSH references
External references:
No OMIM references
1 MeSH reference: D020254

Dental ankylosis

Very frequent
- Anodontia / oligodontia / hypodontia
- Autosomal dominant inheritance

Frequent
- Abnormal dentition / dental position / implantation / unerupted / dental ankylosis
- Enamel anomaly

Occasional
- Clinodactyly of fifth finger
- Prognathism / prognathia


Autosomal dominant nonsyndromic intellectual deficit

(no data available)