Cutis marmorata

Symptom Information:

Symptom ID: HPO:0000965
Synonyms:
Livedo reticularis [HPO:0000965]
Skin marbling [HPO:0000965]
Skin marbling (finding) [Orphanet:23200]
Cutis marmorata (disorder) [Orphanet:23200]
Livedo (finding) [Orphanet:23200]
Livedo reticularis (disorder) [Orphanet:23200]
Cutis marmorata [Orphanet:23200]
Skin marbling [Orphanet:23200]
Livedo Reticularis [Orphanet:23200]
Cutis marmorata [OMIM:Cutis marmorata]
Livedo reticularis [OMIM:Livedo reticularis]
Cutis marmorata/marbled skin/livedo [Orphanet:23200]
Livedo reticularis [Orphanet:23200]
Marbled skin [Orphanet:23200]
Livedo reticularis [MedDRA:10024648]
Mottled skin [MedDRA:10024648]
Cutis marmorata [MedDRA:10024648]
Marbled skin [MedDRA:10024648]
Cutis marmorata (in some patients) [OMIM:Cutis marmorata (in some patients)]
Cutis marmorata (in some) [OMIM:Cutis marmorata (in some)]
Cutis marmorata (rare) [OMIM:Cutis marmorata (rare)]
Livedo [OMIM:Livedo]
Quality:
Cross references:
Orphanet:23200 "Cutis marmorata/marbled skin/livedo" [Orphanet:23200]
OMIM: "Cutis marmorata" [OMIM:Cutis marmorata]
OMIM: "Livedo reticularis" [OMIM:Livedo reticularis]
OMIM: "Cutis marmorata (in some patients)" [OMIM:Cutis marmorata (in some patients)]
OMIM: "Cutis marmorata (in some)" [OMIM:Cutis marmorata (in some)]
OMIM: "Cutis marmorata (rare)" [OMIM:Cutis marmorata (rare)]
OMIM: "Livedo" [OMIM:Livedo]
UMLS:C0263401 "Cutis marmorata" [Orphanet:23200]
UMLS:C1096731 "Skin marbling" [Orphanet:23200]
UMLS:C0085642 "Livedo Reticularis" [Orphanet:23200]
Is a (Direct Parents):
MedDRA Site specific vascular disorders NEC
HPO         Vascular skin abnormality
Orphanet Abnormality of the skin
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)
                   Cutis marmorata(HPO:0000965)
MedDRA:
Vascular disorders(MedDRA:10047065)
    Vascular disorders NEC(MedDRA:10047066)
       Site specific vascular disorders NEC(MedDRA:10057188)
          Cutis marmorata(HPO:0000965)
Database Frequency: 46 / 7739
Resource:

All diseases associated with this symptom:

ADAMS-OLIVER SYNDROME 1 (OMIM:100300)
ADAMS-OLIVER SYNDROME 2 (OMIM:614219)
ADAMS-OLIVER SYNDROME 4 (OMIM:615297)
ANGIOMATOSIS, DIFFUSE CORTICOMENINGEAL, OF DIVRY AND VAN BOGAERT (OMIM:206570)
Adams-Oliver syndrome (Orphanet:974)
Angio-osteohypertrophic syndrome (Orphanet:2346)
BRACHYMESOMELIA-RENAL SYNDROME (OMIM:113470)
Bannayan-Riley-Ruvalcaba syndrome (Orphanet:109)
CHROMOSOME 1p32-p31 DELETION SYNDROME (OMIM:613735)
COFFIN-SIRIS SYNDROME (OMIM:135900)
CORNELIA DE LANGE SYNDROME 1 (OMIM:122470)
CORNELIA DE LANGE SYNDROME 2 (OMIM:300590)
CORNELIA DE LANGE SYNDROME 4 (OMIM:614701)
CORNELIA DE LANGE SYNDROME 5 (OMIM:300882)
Classical homocystinuria (Orphanet:394)
Coffin-Lowry syndrome (Orphanet:192)
Coffin-Siris syndrome (Orphanet:1465)
Cornelia de Lange syndrome (Orphanet:199)
Cutaneous leukocytoclastic angiitis (Orphanet:889)
Cutis marmorata telangiectatica congenita (Orphanet:1556)
Deafness - encephaloneuropathy - obesity - valvulopathy (Orphanet:254898)
Dubowitz syndrome (Orphanet:235)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
Facial dysmorphism - immunodeficiency - livedo - short stature (Orphanet:352712)
Fountain syndrome (Orphanet:3219)
Hypotrichosis - lymphedema - telangiectasia (Orphanet:69735)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
Lethal polymalformative syndrome, Boissel type (Orphanet:210144)
Low birth weight - dwarfism - dysgammaglobulinemia (Orphanet:2621)
MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2 (OMIM:615937)
MOMO syndrome (Orphanet:2563)
MOYAMOYA DISEASE 6 WITH ACHALASIA (OMIM:615750)
Megalencephaly-capillary malformation-polymicrogyria syndrome (Orphanet:60040)
Microscopic polyangiitis (Orphanet:727)
Non-rhizomelic chondrodysplasia punctata (Orphanet:176)
Polyarteritis nodosa (Orphanet:767)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Primary hyperoxaluria (Orphanet:416)
Primary hyperoxaluria type 1 (Orphanet:93598)
Rothmund-Thomson syndrome (Orphanet:2909)
SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION,LETHAL (OMIM:602613)
STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET (OMIM:615934)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Sneddon syndrome (Orphanet:820)
Waldenström macroglobulinemia (Orphanet:33226)
Warsaw breakage syndrome (Orphanet:280558)