MeSH Browser

MeSH Supplementary: Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis
Unique ID: C564570
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564570
Entry Term(s): AMME Complex
Registry Number: 0
Heading Mapped to: *Elliptocytosis, Hereditary; *Intellectual Disability; *Nephritis, Hereditary; *Craniofacial Abnormalities; *Genetic Diseases, X-Linked
Frequency: 2
Date of Entry: 2012/11/05

Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis MeSH Supplementary Concept Data 2024