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Dental ankylosis
1 associated gene
13 connected diseases
6 signs/symptoms
Disease Type of connection
Chondrodysplasia, Blomstrand type
Eiken syndrome
Enchondromatosis
Metaphyseal chondrodysplasia, Jansen type
Brachydactyly type E
Dominant hypophosphatemia with nephrolithiasis or osteoporosis
Familial isolated hypoparathyroidism due to impaired PTH secretion
Autosomal dominant nonsyndromic intellectual deficit
Craniopharyngioma
Desmoid tumor
Hepatocellular carcinoma, childhood-onset
Pilomatrixoma
Catecholaminergic polymorphic ventricular tachycardia
Synonym(s):
- Ankylosis of teeth
Classification (Orphanet):
- Rare genetic disease
- Rare odontologic disease
Classification (ICD10):
- Diseases of the digestive system -
Epidemiological data:
(no data available)
External references:
No OMIM references
1 MeSH reference: D020254
Gene symbol UniProt reference OMIM reference
PTH1R Q03431168468
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