Disease #05516 (HPANBH4 (hyperphenylalaninemia, mild, non-BH4-deficient (HPANBH4)), OMIM:617384)
| Official abbreviation |
HPANBH4 |
| Name |
hyperphenylalaninemia, mild, non-BH4-deficient (HPANBH4) |
| OMIM ID |
617384 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
4 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
DNAJC12 |
| Associated tissues |
- |
| Disease features |
autosomal recessive |
| Remarks |
- |
| Date created |
2018-11-16 15:23:14 +01:00 (CET) |
| Date last edited |
2020-01-06 08:57:05 +01:00 (CET) |
Individuals
|