phosphoribosylpyrophosphate synthetase superactivity
human disease
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Summary
phosphoribosylpyrophosphate synthetase superactivity is a rare disease[1]. It is known by 5 alternative names across languages and contexts.[2]
Key Facts
- phosphoribosylpyrophosphate synthetase superactivity's instance of is recorded as rare disease[3].
- phosphoribosylpyrophosphate synthetase superactivity's instance of is recorded as class of disease[4].
- phosphoribosylpyrophosphate synthetase superactivity is a type of nephropathy secondary to a storage or other metabolic disease[5].
- phosphoribosylpyrophosphate synthetase superactivity is a type of syndromic neurometabolic disease with X-linked intellectual disability[6].
- phosphoribosylpyrophosphate synthetase superactivity is a type of inborn disorder of purine metabolism[7].
- phosphoribosylpyrophosphate synthetase superactivity is a type of X-linked recessive disease[8].
- phosphoribosylpyrophosphate synthetase superactivity is a type of inherited metabolic disorder[9].
- phosphoribosylpyrophosphate synthetase superactivity's genetic association is recorded as PRPS1[10].
- phosphoribosylpyrophosphate synthetase superactivity's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_3222[11].
- phosphoribosylpyrophosphate synthetase superactivity's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111260[12].
- phosphoribosylpyrophosphate synthetase superactivity's exact match is recorded as http://identifiers.org/doid/DOID:0111260[13].
- phosphoribosylpyrophosphate synthetase superactivity's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
Why It Matters
phosphoribosylpyrophosphate synthetase superactivity is known by 5 alternative names across languages and contexts.[2]