The portal for rare diseases and orphan drugs

There is no disease so rare
that it does not deserve attention

Adult pure red cell aplasia

Orpha number	ORPHA98872
Synonym(s)	-
Prevalence	-
Inheritance	-
Age of onset	-

ICD-10	D60.0
OMIM	-
UMLS	-
MeSH	-
MedDRA	-
SNOMED CT	-

Summary

An Orphanet summary for this disease is currently under development. However, other data related to the disease are accessible from the Additional Information menu located on the right side of this page.

Suggest an update

(*) Required fields.

You are (*)

If you have selected the “Other” category, please specify which type of user you are: *

Email address: *

Topic of your comment: *

Epidemiology data

Clinical signs

Nomenclature and/or coding

Attention: Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. For all other comments, please send your remarks via contact us. Only comments written in English can be processed.

Your message * (3000 characters remaining)

Check this box if you wish to receive a copy of your message

Please reproduce the text below

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.