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Ataxia - oculomotor apraxia type 1

1 OMIM reference -
1 associated gene
4 signs/symptoms

PROTEIN INTERACTIONS: 1

Adrenocortical carcinoma

1 OMIM reference -
1 associated gene
No signs/symptoms info

Ataxia - oculomotor apraxia type 1

Adrenocortical carcinoma

(UniProt - OMIM)

(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	APTX	(0.79)	TP53

Citations in the biomedical literature:

Ataxia - oculomotor apraxia type 1		Adrenocortical carcinoma
	Synonym(s): - AOA1		Synonym(s): (no synonyms)

	Classification (Orphanet): - Inborn errors of metabolism - Rare eye disease - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare circulatory system disease - Rare endocrine disease - Rare infertility - Rare oncologic disease - Rare renal disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: sporadic

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D018268

Ataxia - oculomotor apraxia type 1
	Very frequent - Abnormal gait - Ataxia / incoordination / trouble of the equilibrium - Flared eyebrows - Functional anomalies of the nervous system
Adrenocortical carcinoma
(no data available)