Disease #01561 (SPH1 (spherocytosis, type 1 (SPH1)), OMIM:182900)

Official abbreviation SPH1
Name spherocytosis, type 1 (SPH1)
OMIM ID 182900
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease -
Associated with 2 genes ANK1, SPTA1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2020-09-15 10:12:59 +02:00 (CEST)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00448371 - - - M no China - - - - - SPH1 - ANK1 ANK1 1 1 Ke Xu
00448372 - - - F no China - - - - - SPH1 - ANK1 ANK1 1 1 Ke Xu
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