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1 OMIM reference -
1 associated gene
14 signs/symptoms
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Hypodontia - dysplasia of nails
Spinocerebellar ataxia type 17

MSX1 TBP


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
MSX1
(0.89)
TBP



Citations in the biomedical literature:


Hypodontia - dysplasia of nails
MSX1
Spinocerebellar ataxia type 17
TBP



Hypodontia - dysplasia of nails
Spinocerebellar ataxia type 17

Synonym(s):
- Hypodontia - nail dysgenesis
- Tooth and nail syndrome
- Witkop syndrome

Synonym(s):
- HDL4
- Huntington disease-like 4
- SCA17

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

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the nervous system -

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

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

Hypodontia - dysplasia of nails

Very frequent
- Absent / small fingernails / anonychia of hands
- Absent / small toenails / anonychia of feet
- Anodontia / oligodontia / hypodontia
- Anomalies of teeth and dentition
- Autosomal dominant inheritance
- Delayed dentition / eruption of teeth / lack of eruption of teeth
- Dysplastic / thick / grooved fingernails
- Dysplastic / thick / grooved toenails
- Nails anomalies
- Thin / hypoplastic toenails
- Tooth shape anomaly

Frequent
- Everted lower lip
- Fine hair

Occasional
- Abnormal / polycystic ovaries


Spinocerebellar ataxia type 17

(no data available)