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1 OMIM reference -
1 associated gene
9 signs/symptoms
COMMON GENES: 1
3 OMIM references -
16 associated genes
No signs/symptoms info
Hereditary sensory and autonomic neuropathy type 4
Papillary or follicular thyroid carcinoma

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


COMMON
GENES
NTRK1



Citations in the biomedical literature:


Hereditary sensory and autonomic neuropathy type 4
NTRK1
Papillary or follicular thyroid carcinoma
CCDC6 DIRC3 ERC1 FOXE1 GOLGA5 NCOA4
NDUFA13 NKX2-1 PCM1 RET TFG
TPR TRIM24 TRIM27 TRIM33



Hereditary sensory and autonomic neuropathy type 4
Papillary or follicular thyroid carcinoma

Synonym(s):
- HSAN4
- Insensitivity to pain - anhidrosis
- NHSA4

Synonym(s):
- Well-differentiated thyroid carcinoma

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

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
Class of prevalence: unknown
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:
1 OMIM reference -
No MeSH references
External references:
3 OMIM references -
No MeSH references

Hereditary sensory and autonomic neuropathy type 4

Very frequent
- Autosomal recessive inheritance
- Chronic skin infection / ulcerations / ulcers / cancrum
- Insensitivity to pain
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Osteosclerosis / osteopetrosis / bone condensation
- Psychic / behavioural troubles

Occasional
- Dental staining anomaly / spotted teeth / erythrodontia
- Thick skin / pachydermia / orange skin
- Tight skin / lack of elasticity


Papillary or follicular thyroid carcinoma

(no data available)