Sphingosine Phosphate Lyase Insufficiency Syndrome
human disease
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Sphingosine Phosphate Lyase Insufficiency Syndrome
Summary
Sphingosine Phosphate Lyase Insufficiency Syndrome is a class of disease[1].
Key Facts
- Sphingosine Phosphate Lyase Insufficiency Syndrome's instance of is recorded as class of disease[2].
- Sphingosine Phosphate Lyase Insufficiency Syndrome's subclass of is recorded as familial nephrotic syndrome[3].
- Sphingosine Phosphate Lyase Insufficiency Syndrome's subclass of is recorded as autosomal recessive disease[4].
- Sphingosine Phosphate Lyase Insufficiency Syndrome's OMIM ID is recorded as 617575[5].
- Sphingosine Phosphate Lyase Insufficiency Syndrome's Disease Ontology ID is recorded as DOID:0080265[6].
- Sphingosine Phosphate Lyase Insufficiency Syndrome's Orphanet ID is recorded as 506334[7].
- Sphingosine Phosphate Lyase Insufficiency Syndrome's genetic association is recorded as SGPL1[8].
- Sphingosine Phosphate Lyase Insufficiency Syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080265[9].
- Sphingosine Phosphate Lyase Insufficiency Syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_506334[10].
- Sphingosine Phosphate Lyase Insufficiency Syndrome's UMLS CUI is recorded as C4539778[11].
- Sphingosine Phosphate Lyase Insufficiency Syndrome's UMLS CUI is recorded as C5568768[12].
- Sphingosine Phosphate Lyase Insufficiency Syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- Sphingosine Phosphate Lyase Insufficiency Syndrome's Mondo ID is recorded as MONDO_0033203[14].
- Sphingosine Phosphate Lyase Insufficiency Syndrome's UniProt disease ID is recorded as DI-05043[15].