hereditary pyropoikilocytosis
(Q5737872)
An autosomal recessive inherited severe hemolytic anemia. It is a subtype of hereditary elliptocytosis and is characterized by partial spectrin deficiency.
An autosomal recessive inherited severe hemolytic anemia. It is a subtype of hereditary elliptocytosis and is characterized by partial spectrin deficiency.
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Current Data About
hereditary pyropoikilocytosis
| (P31) |
(Q929833)
(Q112193867) |
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| (P279) |
(Q1145668)
(Q2100708) (Q200779)
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| (P1692) |
790.09
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| (P1748) |
C98943
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| (P2293) |
(Q18031690)
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| (P2888) |
http://purl.obolibrary.org/obo/HP_0004839
http://www.orpha.net/ORDO/Orphanet_98867 |
other details
| aliases |
HPP Pyropoikilocytosis hereditary Hereditary Pyropoikilocytosis PYROPOIKILOCYTOSIS, HEREDITARY; HPP PYROPOIKILOCYTOSIS, HEREDITARY |
| description | An autosomal recessive inherited severe hemolytic anemia. It is a subtype of hereditary elliptocytosis and is characterized by partial spectrin deficiency. |
External Links
| (P486) |
C563004
C563004 |
| (P492) |
266140
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| (P665) |
H01125
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| (P1550) |
98867
|
| (P2892) |
C0520739
C0520739 |
| (P3841) |
HP:0004839
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| (P4317) |
4619
|
| (P5270) |
MONDO_0009948
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| (P6366) |
2778988730
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| (P11430) |
DI-01737
|