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2 OMIM references -
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
3 OMIM references -
16 associated genes
No signs/symptoms info
Inherited congenital spastic tetraplegia
Papillary or follicular thyroid carcinoma

ADD3 CCDC6
GAD1 DIRC3
KANK1 ERC1
FOXE1
GOLGA5
NCOA4
NDUFA13
NKX2-1
NTRK1
PCM1
RET
TFG
TPR
TRIM24
TRIM27
TRIM33


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
KANK1
(0.63)
TPR



Citations in the biomedical literature:


Inherited congenital spastic tetraplegia
ADD3 GAD1 KANK1
Papillary or follicular thyroid carcinoma
CCDC6 DIRC3 ERC1 FOXE1 GOLGA5 NCOA4
NDUFA13 NKX2-1 NTRK1 PCM1 RET TFG
TPR TRIM24 TRIM27 TRIM33



Inherited congenital spastic tetraplegia
Papillary or follicular thyroid carcinoma

Synonym(s):
- Inherited congenital spastic quadriplegia

Synonym(s):
- Well-differentiated thyroid carcinoma

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare endocrine disease
- Rare oncologic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Neoplasms -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: sporadic

External references:
2 OMIM references -
No MeSH references
External references:
3 OMIM references -
No MeSH references

No signs/symptoms info available.