MeSH Browser

MeSH Supplementary: Rud Syndrome
Unique ID: C535878
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535878
Entry Term(s): Dwarfism ichthyosiform erythroderma mental deficiency syndrome; Ichthyosis hypogonadism mental retardation epilepsy syndrome; Ichthyosis male hypogonadism syndrome; Ichthyosis mental retardation-epilepsy hypogonadism syndrome; Ichthyosis oligophrenia epilepsy syndrome; Neuroichthyosis hypogonadism syndrome; Rud's syndrome
Registry Number: 0
Heading Mapped to: *Epilepsy; *Hypogonadism; *Ichthyosis; *Intellectual Disability
Frequency: 4
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Rud Syndrome MeSH Supplementary Concept Data 2024