Petechiae
Symptom Information:
Symptom ID: | HPO:0000967 | |||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of blood and blood-forming tissues(HPO:0001871) Abnormal bleeding(HPO:0001892) Subcutaneous hemorrhage(HPO:0001933) Petechiae(HPO:0000967) 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) 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) |
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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) |