Stomatocytosis

Symptom Information:

Symptom ID: HPO:0004446
Synonyms:
erythrocyte stomatocytes [HPO:0004446]
Red cell stomatocytosis [HPO:0004446]
Erythrocyte stomatocytes [OMIM:Erythrocyte stomatocytes]
Red cell stomatocytosis [OMIM:Red cell stomatocytosis]
Stomatocytosis [OMIM:Stomatocytosis]
Quality:
Cross references:
OMIM: "Erythrocyte stomatocytes" [OMIM:Erythrocyte stomatocytes]
OMIM: "Red cell stomatocytosis" [OMIM:Red cell stomatocytosis]
OMIM: "Stomatocytosis" [OMIM:Stomatocytosis]
UMLS:C0272048 "Stomatocytosis" [HPO:0004446]
Is a (Direct Parents):
HPO         Poikilocytosis
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormality of erythrocytes(HPO:0001877)
             Poikilocytosis(HPO:0004447)
                Stomatocytosis(HPO:0004446)
MedDRA:
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

ADENOSINE DEAMINASE, ELEVATED, HEMOLYTIC ANEMIA DUE TO (OMIM:102730)
BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT (OMIM:153670)
Bernard-Soulier syndrome (Orphanet:274)
Familial pseudohyperkalemia (Orphanet:90044)
Mediterranean macrothrombocytopenia (Orphanet:101022)
Overhydrated hereditary stomatocytosis (Orphanet:3203)
PSEUDOHYPERKALEMIA CARDIFF (OMIM:185020)
RHESUS BLOOD GROUP, CcEe ANTIGENS (OMIM:111700)
Rh deficiency syndrome (Orphanet:71275)
SOLUTE CARRIER FAMILY 4 (ANION EXCHANGER), MEMBER 1 (OMIM:109270)
Sitosterolemia (Orphanet:2882)