raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:98865

Homozygous hereditary elliptocytosis

inactive · moved to ORPHA:288Hereditary elliptocytosis

Type
Disease
Group
Disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Hereditary elliptocytosis

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enHomozygous hereditary elliptocytosis
frElliptocytose héréditaire homozygote
deElliptozytose, hereditäre, homozygote
esEliptocitosis hereditaria homocigota
itEllissocitosi ereditaria omozigote
nlHomozygote erfelijke elliptocytose
ptEliptocitose hereditária homozigótica
plHomozygotyczna dziedziczna eliptocytoza
csHomozygotní hereditární eliptocytóza
ukГомозиготний спадковий еліптоцитоз
zh纯合型遗传性椭圆形红细胞增多症
trHomozigot kalıtsal elliptositoz
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Not placed in any Orphanet classification in this release.

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card