Bruising susceptibility

Symptom Information:

Symptom ID: HPO:0000978
Synonyms:
Bruisability [HPO:0000978]
Easy bruisability [HPO:0000978]
Easy bruising [HPO:0000978]
Ecchymoses [HPO:0000978]
Ecchymosis [Orphanet:23620]
Easy bruising [Orphanet:35600]
Ecchymosis (finding) [Orphanet:23620]
Ecchymosis (morphologic abnormality) [Orphanet:23620]
Easy bruising (finding) [Orphanet:35600]
Does bruise easily (situation) [Orphanet:35600]
Increased tendency to bruise [Orphanet:35600]
Bruisability [OMIM:Bruisability]
Easy bruisability [OMIM:Easy bruisability]
Easy bruising [OMIM:Easy bruising]
Ecchymoses [OMIM:Ecchymoses]
Ecchymoses [Orphanet:23620]
Bruisability [Orphanet:35600]
Ecchymosis [MedDRA:10014080]
Ecchymoses [MedDRA:10014080]
Ecchymosis NOS [MedDRA:10014080]
Rash ecchymotic [MedDRA:10014080]
Spontaneous ecchymoses [MedDRA:10014080]
Suggillation [MedDRA:10014080]
Increased tendency to bruise [MedDRA:10021688]
Spontaneous bruising [MedDRA:10021688]
Easy bruising (1 family) [OMIM:Easy bruising (1 family)]
Easy bruising (in some patients) [OMIM:Easy bruising (in some patients)]
Ecchymosis [OMIM:Ecchymosis]
Quality:
Cross references:
Orphanet:23620 "Ecchymoses" [Orphanet:23620]
Orphanet:35600 "Bruisability" [Orphanet:35600]
OMIM: "Bruisability" [OMIM:Bruisability]
OMIM: "Easy bruisability" [OMIM:Easy bruisability]
OMIM: "Easy bruising" [OMIM:Easy bruising]
OMIM: "Ecchymoses" [OMIM:Ecchymoses]
OMIM: "Easy bruising (1 family)" [OMIM:Easy bruising (1 family)]
OMIM: "Easy bruising (in some patients)" [OMIM:Easy bruising (in some patients)]
OMIM: "Ecchymosis" [OMIM:Ecchymosis]
UMLS:C0013491 "Ecchymoses" [HPO:0000978]
UMLS:C0013491 "Ecchymosis" [Orphanet:23620]
UMLS:C0423798 "Increased tendency to bruise" [Orphanet:35600]
Is a (Direct Parents):
HPO         Subcutaneous hemorrhage
Orphanet Vascular skin abnormality
Orphanet Abnormality of cardiovascular system physiology
MedDRA Purpura and related conditions
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Generalized abnormality of skin(HPO:0011354)
                Vascular skin abnormality(HPO:0011276)
                   Subcutaneous hemorrhage(HPO:0001933)
                      Bruising susceptibility(HPO:0000978)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormal bleeding(HPO:0001892)
             Subcutaneous hemorrhage(HPO:0001933)
                Bruising susceptibility(HPO:0000978)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Vascular skin abnormality(HPO:0011276)
       Purpura and related conditions(MedDRA:10037555)
          Bruising susceptibility(HPO:0000978)
Database Frequency: 123 / 7739
Resource:

All diseases associated with this symptom:

ACTH-dependent Cushing syndrome (Orphanet:99892)
ACTH-independent Cushing syndrome (Orphanet:99893)
ACTH-independent macronodular adrenal hyperplasia (Orphanet:189427)
Adiposis dolorosa (Orphanet:36397)
Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16 (Orphanet:98791)
Alpha-thalassemia - myelodysplastic syndrome (Orphanet:231401)
Aneurysm - osteoarthritis syndrome (Orphanet:284984)
Arterial tortuosity syndrome (Orphanet:3342)
Attenuated Chédiak-Higashi syndrome (Orphanet:352723)
Autosomal recessive malignant osteopetrosis (Orphanet:667)
Autosomal thrombocytopenia with normal platelets (Orphanet:168629)
BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT (OMIM:153670)
BLEEDING DISORDER, PLATELET-TYPE, 12 (OMIM:605735)
BLEEDING DISORDER, PLATELET-TYPE, 14 (OMIM:614158)
BLEEDING DISORDER, PLATELET-TYPE, 17 (OMIM:187900)
Bernard-Soulier syndrome (Orphanet:274)
Beta-thalassemia - X-linked thrombocytopenia (Orphanet:231393)
Bleeding diathesis due to a collagen receptor defect (Orphanet:73271)
Bleeding diathesis due to glycoprotein VI deficiency (Orphanet:98885)
Bleeding diathesis due to integrin alpha2-beta1 deficiency (Orphanet:98886)
Bleeding diathesis due to thromboxane synthesis deficiency (Orphanet:220443)
Brittle cornea syndrome (Orphanet:90354)
Chédiak-Higashi syndrome (Orphanet:167)
Congenital alpha2 antiplasmin deficiency (Orphanet:79)
Congenital factor II deficiency (Orphanet:325)
Congenital factor V deficiency (Orphanet:326)
Congenital factor XIII deficiency (Orphanet:331)
Connective tissue disorder due to lysyl hydroxylase-3 deficiency (Orphanet:300284)
Cushing disease (Orphanet:96253)
Cushing syndrome (Orphanet:553)
Cushing syndrome due to ectopic ACTH secretion (Orphanet:99889)
Deafness - lymphedema - leukemia (Orphanet:3226)
Dengue fever (Orphanet:99828)
Diaphyseal medullary stenosis - bone malignancy (Orphanet:85182)
EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1 (OMIM:601776)
Ehlers-Danlos syndrome due to tenascin-X deficiency (Orphanet:230839)
Ehlers-Danlos syndrome type 1 (Orphanet:90309)
Ehlers-Danlos syndrome type 2 (Orphanet:90318)
Ehlers-Danlos syndrome type 7A (Orphanet:99875)
Ehlers-Danlos syndrome type 7B (Orphanet:99876)
Ehlers-Danlos syndrome, arthrochalasic type (Orphanet:1899)
Ehlers-Danlos syndrome, cardiac valvular type (Orphanet:230851)
Ehlers-Danlos syndrome, classic type (Orphanet:287)
Ehlers-Danlos syndrome, dermatosparaxis type (Orphanet:1901)
Ehlers-Danlos syndrome, fibronectinemic type (Orphanet:75501)
Ehlers-Danlos syndrome, kyphoscoliotic and deafness type (Orphanet:300179)
Ehlers-Danlos syndrome, kyphoscoliotic type (Orphanet:1900)
Ehlers-Danlos syndrome, musculocontractural type (Orphanet:2953)
Ehlers-Danlos syndrome, periodontitis type (Orphanet:75392)
Ehlers-Danlos syndrome, spondylocheirodysplastic type (Orphanet:157965)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Epidermolysis bullosa simplex with mottled pigmentation (Orphanet:79397)
Epidermolysis bullosa simplex, Ogna type (Orphanet:79401)
FACTOR XIII, A SUBUNIT, DEFICIENCY OF (OMIM:613225)
FACTOR XIII, B SUBUNIT, DEFICIENCY OF (OMIM:613235)
FACTORS VIII, IX AND XI, COMBINED DEFICIENCY OF (OMIM:134520)
FANCONI ANEMIA, COMPLEMENTATION GROUP A (OMIM:227650)
FANCONI ANEMIA, COMPLEMENTATION GROUP C (OMIM:227645)
FANCONI ANEMIA, COMPLEMENTATION GROUP D2 (OMIM:227646)
FANCONI ANEMIA, COMPLEMENTATION GROUP E (OMIM:600901)
FECHTNER SYNDROME (OMIM:153640)
Familial platelet syndrome with predisposition to acute myelogenous leukemia (Orphanet:71290)
Fanconi anemia (Orphanet:84)
GIANT PLATELET SYNDROME WITH THROMBOCYTOPENIA (OMIM:137560)
Gaucher disease type 1 (Orphanet:77259)
Glanzmann thrombasthenia (Orphanet:849)
Gray platelet syndrome (Orphanet:721)
HEMOPHILIA A (OMIM:306700)
HEMOPHILIA A WITH VASCULAR ABNORMALITY (OMIM:306800)
HERMANSKY-PUDLAK SYNDROME 1 (OMIM:203300)
HERMANSKY-PUDLAK SYNDROME 5 (OMIM:614074)
Hereditary combined deficiency of vitamin K-dependent clotting factors (Orphanet:98434)
Hermansky-Pudlak syndrome (Orphanet:79430)
Hermansky-Pudlak syndrome type 7 (Orphanet:231531)
Hermansky-Pudlak syndrome type 8 (Orphanet:231537)
Hermansky-Pudlak syndrome with pulmonary fibrosis (Orphanet:231500)
INTEGRIN, BETA-3 (OMIM:173470)
Immunoglobulin A vasculitis (Orphanet:761)
LOEYS-DIETZ SYNDROME 4 (OMIM:614816)
LOEYS-DIETZ SYNDROME, TYPE 2A (OMIM:608967)
Localized epidermolysis bullosa simplex (Orphanet:79400)
MACS syndrome (Orphanet:217335)
MAY-HEGGLIN ANOMALY (OMIM:155100)
MYH9-related thrombocytopenia (Orphanet:182050)
Marfan syndrome type 2 (Orphanet:284973)
Marshall-Smith syndrome (Orphanet:561)
Noonan syndrome (Orphanet:648)
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (Orphanet:363972)
ORTHOSTATIC HYPOTENSIVE DISORDER, STREETEN TYPE (OMIM:143850)
OSTEOGENESIS IMPERFECTA, TYPE I (OMIM:166200)
Occipital horn syndrome (Orphanet:198)
Osteogenesis imperfecta type 1 (Orphanet:216796)
Osteopetrosis (Orphanet:2781)
P2Y12 defect (Orphanet:36355)
PASSOVOY FACTOR DEFECT (OMIM:168830)
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1 (OMIM:610489)
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2 (OMIM:610475)
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4 (OMIM:615830)
PLASMA CLOT RETRACTION FACTOR, DEFICIENCY OF (OMIM:262800)
PRIMARY RELEASE DISORDER OF PLATELETS (OMIM:176630)
PURINERGIC RECEPTOR P2X, LIGAND-GATED ION CHANNEL, 1 (OMIM:600845)
PURPURA SIMPLEX (OMIM:179000)
Polycythemia vera (Orphanet:729)
Primary pigmented nodular adrenocortical disease (Orphanet:189439)
Pseudoxanthoma elasticum (Orphanet:758)
Quebec platelet disorder (Orphanet:220436)
RIENHOFF SYNDROME (OMIM:615582)
Rift valley fever (Orphanet:319251)
THROMBOCYTOPENIA 5 (OMIM:616216)
TRAPS syndrome (Orphanet:32960)
Thrombocytopenia with congenital dyserythropoietic anemia (Orphanet:67044)
Tricho-oculo-dermo-vertebral syndrome (Orphanet:3354)
VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1 (OMIM:277450)
Von Willebrand disease type 1 (Orphanet:166078)
Von Willebrand disease type 2 (Orphanet:166081)
Von Willebrand disease type 2A (Orphanet:166084)
Von Willebrand disease type 2B (Orphanet:166087)
Von Willebrand disease type 2M (Orphanet:166090)
Von Willebrand disease type 2N (Orphanet:166093)
Von Willebrand disease type 3 (Orphanet:166096)
Wiskott-Aldrich syndrome (Orphanet:906)
X-linked Ehlers-Danlos syndrome (Orphanet:75497)
X-linked thrombocytopenia with normal platelets (Orphanet:852)