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Human Disease and Mouse Model Detail
Human Disease

Term: Leukodystrophy, Hypomyelinating, 7, with or without Oligodontia and/or Hypogonadotropic Hypogonadism; HLD7
OMIM ID: 607694

Synonyms 4h Syndrome; Ataxia, Delayed Dentition, and Hypomyelination; ADDH; Leukodystrophy, Hypomyelinating, with Hypodontia and Hypogonadotropic Hypogonadism; Leukoencephalopathy, Hypomyelinating, with Ataxia and Delayed Dentition
Associated Genes

Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.

Mouse Gene
Human Gene
 
Characteristics of this human disease are associated with mutations in...
     
Polr3a POLR3A
Polr3b POLR3B
  human...the human gene.
     MGI data currently do not associate this disease with mutations in the orthologous mouse gene.
     
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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Send questions and comments to User Support. 		last database update
04/03/2013
MGI 5.12 		The Jackson Laboratory