Disease #02696 (HLD7 (leukodystrophy, hypomyelinating, type 7 (HLD7)), OMIM:607694)
Official abbreviation |
HLD7 |
Name |
leukodystrophy, hypomyelinating, type 7 (HLD7) |
OMIM ID |
607694 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
2 |
Phenotype entries for this disease |
2 |
Associated with 1 gene |
POLR3A |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-01-15 19:28:31 +01:00 (CET) |
Individuals
|