Disease #00119 (MC2DN4 (MITOCHONDRIAL COMPLEX II DEFICIENCY, NUCLEAR TYPE 4), OMIM:619224)
Official abbreviation |
MC2DN4 |
Name |
MITOCHONDRIAL COMPLEX II DEFICIENCY, NUCLEAR TYPE 4 |
OMIM ID |
619224 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
SDHB |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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