Petechiae

Symptom Information:

Symptom ID: HPO:0000967
Synonyms:
Skin petechia [Orphanet:23610]
Petechia [HPO:0000967]
Petechiae of skin (disorder) [Orphanet:23610]
Petechiae (finding) [Orphanet:23610]
Petechia (morphologic abnormality) [Orphanet:23610]
Petechiae [Orphanet:23610]
Petechiae [OMIM:Petechiae]
Purpura/petichiae [Orphanet:23610]
Petechiae [MedDRA:10034754]
Petechia [MedDRA:10034754]
Petechial rash [MedDRA:10034754]
Rash petechial [MedDRA:10034754]
Capillary haemorrhage [MedDRA:10034754]
Capillary hemorrhage [MedDRA:10034754]
Petechiae (less common) [OMIM:Petechiae (less common)]
Mucosa purpura [Orphanet:23610]
Purpura (morphologic abnormality) [Orphanet:23610]
Mucosa petechia [Orphanet:23610]
Purpuras (excl thrombocytopenic) [MedDRA:10037550]
Quality:
Cross references:
Orphanet:23610 "Purpura/petichiae" [Orphanet:23610]
OMIM: "Petechiae" [OMIM:Petechiae]
OMIM: "Petechiae (less common)" [OMIM:Petechiae (less common)]
UMLS:C0031256 "Petechiae" [HPO:0000967]
UMLS:C0031256 "Petechiae" [Orphanet:23610]
Is a (Direct Parents):
Orphanet Vascular skin abnormality
MedDRA Purpura and related conditions
HPO         Subcutaneous hemorrhage
MedDRA Coagulopathies and bleeding diatheses (excl thrombocytopenic)
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)
                      Petechiae(HPO:0000967)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormal bleeding(HPO:0001892)
             Subcutaneous hemorrhage(HPO:0001933)
                Petechiae(HPO:0000967)
MedDRA:
Blood and lymphatic system disorders(MedDRA:10005329)
    Coagulopathies and bleeding diatheses (excl thrombocytopenic)(MedDRA:10064477)
       Petechiae(HPO:0000967)
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Vascular skin abnormality(HPO:0011276)
       Purpura and related conditions(MedDRA:10037555)
          Petechiae(HPO:0000967)
Database Frequency: 26 / 7739
Resource:

All diseases associated with this symptom:

AICARDI-GOUTIERES SYNDROME 1 (OMIM:225750)
AL amyloidosis (Orphanet:85443)
Arterial calcification, generalized, of infancy, 1 (OMIM:208000)
Autosomal dominant macrothrombocytopenia (Orphanet:140957)
BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT (OMIM:153670)
Bernard-Soulier syndrome (Orphanet:274)
Beta-thalassemia - X-linked thrombocytopenia (Orphanet:231393)
Congenital intrauterine infection-like syndrome (Orphanet:1229)
Cushing syndrome (Orphanet:553)
Ehlers-Danlos syndrome, fibronectinemic type (Orphanet:75501)
Ethylmalonic encephalopathy (Orphanet:51188)
Fetal Gaucher disease (Orphanet:85212)
Gaucher disease type 1 (Orphanet:77259)
Gaucher disease type 2 (Orphanet:77260)
Gaucher disease type 3 (Orphanet:77261)
Leukocyte adhesion deficiency type III (Orphanet:99844)
MELAS (Orphanet:550)
Neonatal hemochromatosis (Orphanet:446)
PURINERGIC RECEPTOR P2X, LIGAND-GATED ION CHANNEL, 1 (OMIM:600845)
Primary systemic amyloidosis (Orphanet:314701)
Prolidase deficiency (Orphanet:742)
Radio-ulnar synostosis - amegakaryocytic thrombocytopenia (Orphanet:71289)
THROMBOCYTOPENIA 5 (OMIM:616216)
Thrombocytopenia with congenital dyserythropoietic anemia (Orphanet:67044)
WISKOTT-ALDRICH SYNDROME (OMIM:301000)
X-linked thrombocytopenia with normal platelets (Orphanet:852)