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
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