PLATELET DISORDER, UNDEFINED

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 9
OrphanetNr:
OMIM Id: 173420
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Autosomal dominant inheritance
[Omim]
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
 (HPO:0003006) Neuroblastoma 16 / 7739
2
 (HPO:0003540) Impaired platelet aggregation 17 / 7739
3
 (HPO:0001873) Thrombocytopenia 224 / 7739
4
 (HPO:0003010) Prolonged bleeding time 88 / 7739
5
 (HPO:0001892) Abnormal bleeding 85 / 7739
6
 (HPO:0004377) Hematological neoplasm 12 / 7739
7
 (HPO:0000006) Autosomal dominant inheritance 2518 / 7739
8
 (MedDRA:10066476) Haematological malignancy 1 / 7739
9
 (OMIM) Normal platelet survival time 1 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: