Disease #01789 (folate malabsorption, hereditary, OMIM:229050)

Official abbreviation -
Name folate malabsorption, hereditary
OMIM ID 229050
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 10
Phenotype entries for this disease 0
Associated with 1 gene SLC46A1
Associated tissues -
Disease features -
Remarks -


Individuals

10 entries on 1 page. Showing entries 1 - 10.
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00206422 - - - - - - - - 0 - - folate malabsorption, hereditary - SLC46A1 SLC46A1 1 1 SIB - Livia Famiglietti
00206423 - - - - - - - - 0 - - folate malabsorption, hereditary - SLC46A1 SLC46A1 1 1 SIB - Livia Famiglietti
00206424 - - - - - - - - 0 - - folate malabsorption, hereditary - SLC46A1 SLC46A1 1 1 SIB - Livia Famiglietti
00206425 - - - - - - - - 0 - - folate malabsorption, hereditary - SLC46A1 SLC46A1 1 1 SIB - Livia Famiglietti
00206426 - - - - - - - - 0 - - folate malabsorption, hereditary - SLC46A1 SLC46A1 1 1 SIB - Livia Famiglietti
00206427 - - - - - - - - 0 - - folate malabsorption, hereditary - SLC46A1 SLC46A1 1 1 SIB - Livia Famiglietti
00206428 - - - - - - - - 0 - - folate malabsorption, hereditary - SLC46A1 SLC46A1 1 1 SIB - Livia Famiglietti
00206429 - - - - - - - - 0 - - folate malabsorption, hereditary - SLC46A1 SLC46A1 1 1 SIB - Livia Famiglietti
00206430 - - - - - - - - 0 - - folate malabsorption, hereditary - SLC46A1 SLC46A1 1 1 SIB - Livia Famiglietti
00206431 - - - - - - - - 0 - - folate malabsorption, hereditary - SLC46A1 SLC46A1 1 1 SIB - Livia Famiglietti
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