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
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