Disease #03174 (SPH4 (spherocytosis, type 4 (SPH4)), OMIM:612653)

Official abbreviation SPH4
Name spherocytosis, type 4 (SPH4)
OMIM ID 612653
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 8
Phenotype entries for this disease -
Associated with 1 gene SLC4A1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2020-09-15 10:15:54 +02:00 (CEST)


Individuals

8 entries on 1 page. Showing entries 1 - 8.
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00310045 - - - M no Tunisia - - - - - SPH4 - SLC4A1 SLC4A1 1 1 Nawel Trabelsi
00316201 - - - M yes Tunisia - - - - - SPH4 - SLC4A1 SLC4A1 1 1 Nawel Trabelsi
00318190 - - - - - - - - - - - SPH4 - SLC4A1 SLC4A1 1 2 Nawel Trabelsi
00318192 - - - - - Tunisia - - - - - SPH4 - SLC4A1 SLC4A1 1 1 Nawel Trabelsi
00318193 - - - - - Tunisia - - - - - SPH4 - SLC4A1 SLC4A1 1 1 Nawel Trabelsi
00318194 - - - - - Tunisia - - - - - SPH4 - SLC4A1 SLC4A1 1 1 Nawel Trabelsi
00319387 - - - - - Tunisia - - - - - SPH4 - SLC4A1 SLC4A1 1 1 Nawel Trabelsi
00319895 - - - - - Tunisia - - - - - SPH4 - SLC4A1 SLC4A1 1 1 Nawel Trabelsi
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