Acrocyanosis
Symptom Information:
Symptom ID: | HPO:0001063 | |||||||||||||||||||||||||||
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 the respiratory system(HPO:0002086) Functional respiratory abnormality(HPO:0002795) Cyanosis(HPO:0000961) Acrocyanosis(HPO:0001063) Abnormality of the integument(HPO:0001574) Abnormality of the skin(HPO:0000951) Generalized abnormality of skin(HPO:0011354) Dermatological manifestations of systemic disorders(HPO:0001005) Cyanosis(HPO:0000961) Acrocyanosis(HPO:0001063) MedDRA: Vascular disorders(MedDRA:10047065) Vascular disorders NEC(MedDRA:10047066) Peripheral vascular disorders NEC(MedDRA:10034638) Acrocyanosis(HPO:0001063) |
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Database Frequency: | 56 / 7739 | |||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
AICARDI-GOUTIERES SYNDROME 1 | (OMIM:225750) |
Antisynthetase syndrome | (Orphanet:81) |
Atypical Rett syndrome | (Orphanet:3095) |
Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures | (Orphanet:73229) |
Behçet disease | (Orphanet:117) |
Buerger disease | (Orphanet:36258) |
Bullous dystrophy, macular type | (Orphanet:1867) |
CRYOFIBRINOGENEMIA, FAMILIAL PRIMARY | (OMIM:123540) |
Camurati-Engelmann disease | (Orphanet:1328) |
Cerebroretinal vasculopathy | (Orphanet:3421) |
Cogan syndrome | (Orphanet:1467) |
Combined oxidative phosphorylation defect type 4 | (Orphanet:254925) |
Congenital pulmonary lymphangiectasia | (Orphanet:2414) |
Criss-cross heart | (Orphanet:1461) |
Cryoglobulinemic vasculitis | (Orphanet:91138) |
Cutaneous lupus erythematosus | (Orphanet:535) |
Dermatomyositis | (Orphanet:221) |
Diffuse cutaneous systemic sclerosis | (Orphanet:220393) |
Diffuse palmoplantar keratoderma-acrocyanosis syndrome | (Orphanet:86918) |
Ehlers-Danlos syndrome, classic type | (Orphanet:287) |
Ehlers-Danlos syndrome, hypermobility type | (Orphanet:285) |
Ehlers-Danlos syndrome, vascular type | (Orphanet:286) |
Eosinophilic fasciitis | (Orphanet:3165) |
Eosinophilic granulomatosis with polyangiitis | (Orphanet:183) |
Essential thrombocythemia | (Orphanet:3318) |
Familial dysautonomia | (Orphanet:1764) |
Fucosidosis | (Orphanet:349) |
Giant cell arteritis | (Orphanet:397) |
HEMANGIOMATOSIS, CUTANEOUS, WITH ASSOCIATED FEATURES | (OMIM:234800) |
HERNS syndrome | (Orphanet:63261) |
Hereditary vascular retinopathy | (Orphanet:71291) |
Hutchinson-Gilford progeria syndrome | (Orphanet:740) |
Hyperimmunoglobulinemia D with periodic fever | (Orphanet:343) |
Hypocomplementemic urticarial vasculitis | (Orphanet:36412) |
Idiopathic pulmonary alveolar proteinosis | (Orphanet:747) |
Limited cutaneous systemic sclerosis | (Orphanet:220402) |
Microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome | (Orphanet:329332) |
Mixed connective tissue disease | (Orphanet:809) |
Monomelic amyotrophy | (Orphanet:65684) |
Neuralgic amyotrophy | (Orphanet:2901) |
Peripheral motor neuropathy - dysautonomia | (Orphanet:2400) |
Polyarteritis nodosa | (Orphanet:767) |
Primary hyperoxaluria | (Orphanet:416) |
Primary hyperoxaluria type 1 | (Orphanet:93598) |
Pulmonary arterial hypertension | (Orphanet:182090) |
Pulmonary atresia - intact ventricular septum | (Orphanet:1208) |
Retinal vasculopathy and cerebral leukodystrophy | (Orphanet:247691) |
Reynolds syndrome | (Orphanet:779) |
Rombo syndrome | (Orphanet:3110) |
Scleroderma | (Orphanet:801) |
Secondary polycythemia | (Orphanet:98428) |
Sneddon syndrome | (Orphanet:820) |
Systemic sclerosis | (Orphanet:90291) |
Thoracic outlet syndrome | (Orphanet:97330) |
Thymic tumor | (Orphanet:100100) |
Waardenburg syndrome type 3 | (Orphanet:896) |