Malouf syndrome
This syndrome is characterized by the association of dilated cardiomyopathy and hypergonadotropic hypogonadism (DCM-HH)
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Malouf syndrome
Summary
Malouf syndrome is a rare disease[1].
Key Facts
- Malouf syndrome's instance of is recorded as rare disease[2].
- Malouf syndrome's instance of is recorded as class of disease[3].
- Malouf syndrome is a type of dilated cardiomyopathy[4].
- Malouf syndrome is a type of syndrome associated with dilated cardiomyopathy[5].
- Malouf syndrome is a type of hypergonadotropic hypogonadism[6].
- Malouf syndrome is a type of syndrome[7].
- Malouf syndrome is a type of autosomal dominant disease[8].
- Malouf syndrome's NCI Thesaurus ID is recorded as C174217[9].
- Malouf syndrome's genetic association is recorded as LMNA[10].
- Malouf syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2229[11].
- Malouf syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111584[12].
- Malouf syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111584[13].