myoglobinuria, acute recurrent, autosomal recessive
human disease
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myoglobinuria, acute recurrent, autosomal recessive
Summary
myoglobinuria, acute recurrent, autosomal recessive is a class of disease[1].
Key Facts
- myoglobinuria, acute recurrent, autosomal recessive's instance of is recorded as class of disease[2].
- myoglobinuria, acute recurrent, autosomal recessive's subclass of is recorded as myoglobinuria, recurrent[3].
- myoglobinuria, acute recurrent, autosomal recessive's subclass of is recorded as muscular lipidosis[4].
- myoglobinuria, acute recurrent, autosomal recessive's MeSH descriptor ID is recorded as C564832[5].
- myoglobinuria, acute recurrent, autosomal recessive's OMIM ID is recorded as 268200[6].
- myoglobinuria, acute recurrent, autosomal recessive's KEGG ID is recorded as H01290[7].
- myoglobinuria, acute recurrent, autosomal recessive's Orphanet ID is recorded as 99845[8].
- myoglobinuria, acute recurrent, autosomal recessive's genetic association is recorded as LPIN1[9].
- myoglobinuria, acute recurrent, autosomal recessive's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_99845[10].
- myoglobinuria, acute recurrent, autosomal recessive's UMLS CUI is recorded as C1849386[11].
- myoglobinuria, acute recurrent, autosomal recessive's ICD-10-CM is recorded as R82.1[12].
- myoglobinuria, acute recurrent, autosomal recessive's Mondo ID is recorded as MONDO_0020504[13].
- myoglobinuria, acute recurrent, autosomal recessive's UniProt disease ID is recorded as DI-01227[14].