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

4 entries on 1 page. Showing entries 1 - 4.
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00180961 - Journal: Gallego 2020 - M - Spain - - - - - HPANBH4 hyperphenylalaninemia (HP:0004923) DNAJC12 DNAJC12 1 1 Belen Perez
00287088 - Journal: Gallego 2020 - - - - - - - - - HPANBH4 - DNAJC12 DNAJC12 2 1 Belen Perez
00287089 - Journal: Gallego 2020 - - - - - - - - - HPANBH4 - DNAJC12 DNAJC12 2 1 Belen Perez
00288258 - Journal: Gallego 2020 - - - - - - - - - HPANBH4 - DNAJC12 DNAJC12 2 1 Belen Perez
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