Disease #01833 (HPABH4B (Hyperphenylalaninemia, BH4-deficient, B), OMIM:233910)
Official abbreviation |
HPABH4B |
Name |
Hyperphenylalaninemia, BH4-deficient, B |
OMIM ID |
233910 |
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 |
GCH1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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