Cutis marmorata
Symptom Information:
Symptom ID: | HPO:0000965 | ||||||||||||||||||||||
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 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) |
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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) |