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MCID: RVN001
MIFTS: 13
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Ravine Syndrome
Categories:
Neuronal diseases, Rare diseases
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MalaCards integrated aliases for Ravine Syndrome:
Name: Ravine Syndrome
58
Characteristics:Orphanet epidemiological data:58
ravine syndrome
Inheritance: Autosomal recessive; Prevalence: <1/1000000 (Worldwide); Age of onset: Infancy; Classifications:
ICD10:
33
Orphanet: 58
Rare neurological diseases |
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MalaCards based summary :
Ravine Syndrome, is also known as reunion island-anorexia-vomiting which is irrepressible-neurological signs syndrome. An important gene associated with Ravine Syndrome is SLC7A2-IT1 (SLC7A2 Intronic Transcript 1). Affiliated tissues include eye, and related phenotypes are failure to thrive and anorexia
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Human phenotypes related to Ravine Syndrome:58 31 (showing 14, show less)
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MalaCards organs/tissues related to Ravine Syndrome:40
Eye
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Genes related to Ravine Syndrome (1 elite genes):(showing 1, show less) - Elite gene
- Cancer Census gene in COSMIC
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Search
GEO
for disease gene expression data for Ravine Syndrome.
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