Disease #04135 (PELD (encephalopathy, progressive, with/without lipodystrophy (PELD)), OMIM:615924)
Official abbreviation |
PELD |
Name |
encephalopathy, progressive, with/without lipodystrophy (PELD) |
OMIM ID |
615924 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
BSCL2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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