ODCs

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2 OMIM references -
3 associated genes
18 signs/symptoms

PROTEIN INTERACTIONS: 1

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

Cerebellar ataxia - hypogonadism

Familial platelet syndrome with predisposition to acute myelogenous leukemia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	STUB1	(0.68)	RUNX1

Citations in the biomedical literature:

Cerebellar ataxia - hypogonadism		Familial platelet syndrome with predisposition to acute myelogenous leukemia
	Synonym(s): - Luteinizing hormone-releasing hormone deficiency with ataxia		Synonym(s): - FPD/AML syndrome - FPS/AML syndrome - Familial platelet disorder with associated myeloid malignancy - Familial platelet syndrome

	Classification (Orphanet): - Rare endocrine disease - Rare genetic disease - Rare gynecologic or obstetric disease - Rare infertility - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare hematologic disease - Rare oncologic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

	Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: no data available Average age of death: no data available Type of inheritance: autosomal dominant

	External references: 2 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

Cerebellar ataxia - hypogonadism
	Very frequent - Abnormal ERG / electroretinogram / electroretinography - Ataxia / incoordination / trouble of the equilibrium - Gynecomastia / breast / mammary gland enlargement / hyperplasia - Hypothalamic-hypophyseal axis anomalies / hypothalamus / pituitary anomalies - Late puberty / hypogonadism / hypogenitalism - Nystagmus - Optic nerve anomaly / optic atrophy / anomaly of the papilla - Retinitis pigmentosa / retinal pigmentary changes - Speech troubles / aphasia / dysphasia / echolalia / mutism / logorrhea / dysprosodia - Sterility / hypofertility Frequent - Hemiplegia / diplegia / hemiparesia / limb palsy - Hypotonia Occasional - Brachycephaly / flat occiput - Clinodactyly of fifth finger - Psychic / behavioural troubles - Psychic / psychomotor regression / dementia / intellectual decline - Short stature / dwarfism / nanism - Supernumerary nipples / polythelia
Familial platelet syndrome with predisposition to acute myelogenous leukemia
(no data available)