Malouf syndrome

Summary

Malouf syndrome is a rare disease^[1]. It draws 12 Wikipedia views per month (rare_disease category, ranking #229 of 627).^[2]

Key Facts

• Malouf syndrome's instance of is recorded as rare disease^[3].
• Malouf syndrome's instance of is recorded as class of disease^[4].
• Malouf syndrome's subclass of is recorded as dilated cardiomyopathy^[5].
• Malouf syndrome's subclass of is recorded as syndrome associated with dilated cardiomyopathy^[6].
• Malouf syndrome's subclass of is recorded as hypergonadotropic hypogonadism^[7].
• Malouf syndrome's subclass of is recorded as syndrome^[8].
• Malouf syndrome's subclass of is recorded as autosomal dominant disease^[9].
• Malouf syndrome's OMIM ID is recorded as 212112^[10].
• Malouf syndrome's Disease Ontology ID is recorded as DOID:0111584^[11].
• Malouf syndrome's Orphanet ID is recorded as 2229^[12].
• Malouf syndrome's NCI Thesaurus ID is recorded as C174217^[13].
• Malouf syndrome's genetic association is recorded as LMNA^[14].
• Malouf syndrome's Google Knowledge Graph ID is recorded as /g/122l88p8^[15].
• Malouf syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2229^[16].
• Malouf syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111584^[17].
• Malouf syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111584^[18].
• Malouf syndrome's UMLS CUI is recorded as C0796031^[19].
• Malouf syndrome's UMLS CUI is recorded as C0796083^[20].
• Malouf syndrome's ICD-10-CM is recorded as Q87.8^[21].
• Malouf syndrome's Mondo ID is recorded as MONDO_0008915^[22].
• Malouf syndrome's Microsoft Academic ID is recorded as 2776985822^[23].
• Malouf syndrome's UniProt disease ID is recorded as DI-02906^[24].

Why It Matters

Malouf syndrome draws 12 Wikipedia views per month (rare_disease category, ranking #229 of 627).^[2]