| Human Disease |
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 | |||||||||||||||||||||||||
|
Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
|
|||||||||||||||||||||||||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
||
|
Citing These Resources Funding Information Warranty Disclaimer & Copyright Notice Send questions and comments to User Support. |
last database update 05/08/2013 MGI 5.13 |
|
|
|
||