Acrocyanosis

Symptom Information:

Symptom ID: HPO:0001063
Synonyms:
Acrocyanosis (finding) [Orphanet:35270]
Acrocyanosis [Orphanet:35270]
Acrocyanosis [OMIM:Acrocyanosis]
Acrocyanosis/Raynaud's phenomenon/vasomotor disorders [Orphanet:35270]
Cyanosis [MedDRA:10011703]
Acrocyanosis [MedDRA:10011703]
Blue lips [MedDRA:10011703]
Cyanosed [MedDRA:10011703]
Cyanosis NOS [MedDRA:10011703]
Cyanosis of lip [MedDRA:10011703]
Cyanosis peripheral [MedDRA:10011703]
Cyanotic [MedDRA:10011703]
Lips cyanosed [MedDRA:10011703]
Nails cyanosed [MedDRA:10011703]
Circumoral cyanosis [MedDRA:10011703]
Cyanosis aggravated [MedDRA:10011703]
Cyanosis (25%) [OMIM:Cyanosis (25%)]
Cyanosis (e.g. Hb M Saskatoon 141900.0165) [OMIM:Cyanosis (e.g. Hb M Saskatoon 141900.0165)]
Vasomotor disorder [Orphanet:35270]
Raynaud's phenomenon [MedDRA:10037912]
Raynaud phenomenon [Orphanet:35270]
Raynaud's phenomenon (finding) [Orphanet:35270]
Raynaud's disease (disorder) [Orphanet:35270]
Raynaud Phenomenon [Orphanet:35270]
Raynaud Disease [Orphanet:35270]
Raynaud phenomenon [OMIM:Raynaud phenomenon]
Raynaud's phenomenon [OMIM:Raynaud's phenomenon]
Quality:
Cross references:
Orphanet:35270 "Acrocyanosis/Raynaud's phenomenon/vasomotor disorders" [Orphanet:35270]
OMIM: "Acrocyanosis" [OMIM:Acrocyanosis]
OMIM: "Cyanosis (25%)" [OMIM:Cyanosis (25%)]
OMIM: "Cyanosis (e.g. Hb M Saskatoon 141900.0165)" [OMIM:Cyanosis (e.g. Hb M Saskatoon 141900.0165)]
OMIM: "Raynaud phenomenon" [OMIM:Raynaud phenomenon]
OMIM: "Raynaud's phenomenon" [OMIM:Raynaud's phenomenon]
UMLS:C0221347 "Acrocyanosis" [HPO:0001063]
UMLS:C0221347 "Acrocyanosis" [Orphanet:35270]
UMLS:C0034735 "Raynaud Phenomenon" [Orphanet:35270]
UMLS:C0034734 "Raynaud Disease" [Orphanet:35270]
Is a (Direct Parents):
MedDRA Peripheral vascular disorders NEC
HPO         Cyanosis
Orphanet Abnormality of cardiovascular system physiology
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)
                Dermatological manifestations of systemic disorders(HPO:0001005)
                   Cyanosis(HPO:0000961)
                      Acrocyanosis(HPO:0001063)
       Abnormality of the respiratory system(HPO:0002086)
          Functional respiratory abnormality(HPO:0002795)
             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)
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)
Beh├žet 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)