RETICULOENDOTHELIOSIS, X-LINKED

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 7
OrphanetNr:
OMIM Id: 312500
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset: Infantile onset
[Omim]

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
 (HPO:0001433) Hepatosplenomegaly 78 / 7739
2
 (HPO:0000952) Jaundice 105 / 7739
3
 (HPO:0001903) Anemia 289 / 7739
4
 (HPO:0002716) Lymphadenopathy 129 / 7739
5
 (HPO:0001417) X-linked inheritance 173 / 7739
6
 (OMIM) Malignant reticuloendotheliosis 1 / 7739
7
 (HPO:0003593) Infantile onset 249 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: