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Term:
multiple cutaneous and mucosal venous malformations (DOID:0050792)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1)
Parent Terms Term With Siblings Child Terms
skin disease +     
vein disease +     
abdominal obesity-metabolic syndrome +   
ablepharon macrostomia syndrome  
Achenbach syndrome 
achondrogenesis type II  
Acneiform Eruptions +   
acrofacial dysostosis Cincinnati type  
acrokeratosis verruciformis  
adiaspiromycosis 
ADULT syndrome  
adult-onset autosomal dominant demyelinating leukodystrophy  
advanced sleep phase syndrome +   
age related macular degeneration +   
Alexander Disease  
allergic cutaneous vasculitis +   
Alzheimer's disease 1 +   
Alzheimer's disease 2  
Alzheimer's disease 3 +   
Alzheimer's disease 4  
Alzheimer's disease 5 
amelogenesis imperfecta type 1A  
amelogenesis imperfecta type 1B  
amelogenesis imperfecta type 3A  
amelogenesis imperfecta type 3B  
amelogenesis imperfecta type 4  
ancylostomiasis +  
Andersen-Tawil syndrome  
angioedema +   
ankyloblepharon-ectodermal defects-cleft lip/palate syndrome  
APP-related cerebral amyloid angiopathy  
arrhythmogenic right ventricular dysplasia 1  
arrhythmogenic right ventricular dysplasia 10  
arrhythmogenic right ventricular dysplasia 11  
arrhythmogenic right ventricular dysplasia 12  
arrhythmogenic right ventricular dysplasia 13  
arrhythmogenic right ventricular dysplasia 2  
arrhythmogenic right ventricular dysplasia 3 
arrhythmogenic right ventricular dysplasia 4 
arrhythmogenic right ventricular dysplasia 5  
arrhythmogenic right ventricular dysplasia 8  
arrhythmogenic right ventricular dysplasia 9  
Arteriovenous Fistula +   
arteriovenous malformations of the brain +   
atrial heart septal defect 2  
atrial heart septal defect 5  
atrial heart septal defect 6  
atrial heart septal defect 7  
atrial heart septal defect 8  
atrial heart septal defect 9  
autoimmune lymphoproliferative syndrome type 2A  
autoimmune lymphoproliferative syndrome type 4  
autosomal dominant Alport syndrome  
autosomal dominant cerebellar ataxia +   
autosomal dominant chondrodysplasia punctata +  
autosomal dominant chronic granulomatous disease 
autosomal dominant cutis laxa +   
Autosomal Dominant Dyskeratosis Congenita +   
autosomal dominant Emery-Dreifuss muscular dystrophy 4  
autosomal dominant Emery-Dreifuss muscular dystrophy 5  
autosomal dominant Emery-Dreifuss muscular dystrophy 7  
autosomal dominant familial periodic fever  
autosomal dominant hypocalcemia +   
autosomal dominant hypophosphatemic rickets  
autosomal dominant isolated ectopia lentis 1  
autosomal dominant keratitis-ichthyosis-deafness syndrome  
autosomal dominant limb-girdle muscular dystrophy +   
autosomal dominant macrothrombocytopenia TUBB1-related  
autosomal dominant mental retardation 55  
autosomal dominant mental retardation 56  
autosomal dominant microcephaly +   
autosomal dominant nocturnal frontal lobe epilepsy +   
autosomal dominant non-syndromic intellectual disability +   
autosomal dominant nonsyndromic deafness +   
autosomal dominant osteopetrosis 1  
autosomal dominant osteopetrosis 2  
autosomal dominant Parkinson's disease 1  
autosomal dominant Parkinson's disease 4  
autosomal dominant Parkinson's disease 8  
autosomal dominant polycystic kidney disease +   
autosomal dominant pseudohypoaldosteronism type 1  
autosomal dominant Robinow syndrome 1  
autosomal dominant Robinow syndrome 2  
autosomal dominant Robinow syndrome 3  
autosomal dominant sensory ataxia 1  
autosomal dominant sideroblastic anemia 4  
autosomal dominant type IV Ehlers-Danlos syndrome +   
Axenfeld-Rieger syndrome +   
Bannayan-Riley-Ruvalcaba syndrome  
Bart-Pumphrey syndrome  
Beare-Stevenson cutis gyrata syndrome  
Birk-Barel syndrome  
Birt-Hogg-Dube syndrome  
Blau syndrome  
blepharocheilodontic syndrome +   
blepharophimosis, ptosis, and epicanthus inversus syndrome  
blue color blindness  
Boudhina Yedes Khiari syndrome 
brachydactyly type A1 +   
brachydactyly type A2  
brachydactyly type C  
brachydactyly type D  
branchiooculofacial syndrome  
branchiootorenal syndrome +   
breast disease +   
Brooke-Spiegler syndrome  
Brown-Vialetto-Van Laere syndrome +   
Brugada syndrome 1  
Brugada syndrome 7  
Brugada syndrome 9  
bullous congenital ichthyosiform erythroderma  
CADASIL 1  
CADASIL 2  
campomelic dysplasia +   
Capillary Malformation-Arteriovenous Malformation +   
Carney complex +   
cercarial dermatitis 
chancroid +  
Charcot-Marie-Tooth disease dominant intermediate A 
Charcot-Marie-Tooth disease dominant intermediate B +   
Charcot-Marie-Tooth disease dominant intermediate C  
Charcot-Marie-Tooth disease dominant intermediate D  
Charcot-Marie-Tooth disease dominant intermediate E  
Charcot-Marie-Tooth disease dominant intermediate F  
cherubism +   
chronic ulcer of skin +   
CLAPO Syndrome 
Clouston syndrome  
coenurosis 
contagious pustular dermatitis 
Costello syndrome  
Cowden syndrome +   
Crouzon syndrome-acanthosis nigricans syndrome  
Culler-Jones syndrome  
Cutaneous Fistula 
cutaneous lupus erythematosus +   
cutis laxa +   
Denys-Drash syndrome  
Dermal Fibrosis  
dermatitis +   
Dermatoleukodystrophy 
dermatomyositis +   
dipetalonemiasis 
Duane-radial ray syndrome  
Duplication of Eyebrows with Stretchable Skin and Syndactyly 
dysplastic nevus syndrome +   
Ectodermal Dysplasia-Skin Fragility Syndrome  
Eczematous Skin Diseases +   
EEC syndrome +   
Elastosis Perforans Serpiginosa 
Elliott Ludman Teebi Syndrome 
endometriosis in scar of skin 
epidermal nevus +   
epidermolytic hyperkeratosis +   
Erythema +   
erythematosquamous dermatosis 
esophageal varix  
exanthem +   
FACES Syndrome 
facial dermatosis +   
Facial Ectodermal Dysplasia  
familial cold autoinflammatory syndrome 4  
familial erythrocytosis 1  
familial erythrocytosis 3  
familial erythrocytosis 5  
Feingold syndrome +   
filariasis +   
Flynn Aird Syndrome 
Focal Facial Dermal Dysplasia 4  
Foot Diseases +   
Frasier syndrome  
Genetic Skin Diseases +   
granulomatosis with polyangiitis +   
hair disease +   
Hajdu-Cheney syndrome  
hand dermatosis +  
hand-foot-genital syndrome  
hemorrhoid +   
hereditary breast ovarian cancer syndrome +   
hereditary hemorrhagic telangiectasia +   
hereditary spastic paraplegia 10  
hereditary spastic paraplegia 12  
hereditary spastic paraplegia 13  
hereditary spastic paraplegia 19 
hereditary spastic paraplegia 29 
hereditary spastic paraplegia 31  
hereditary spastic paraplegia 33  
hereditary spastic paraplegia 36 
hereditary spastic paraplegia 37 
hereditary spastic paraplegia 38 
hereditary spastic paraplegia 3A  
hereditary spastic paraplegia 4  
hereditary spastic paraplegia 41 
hereditary spastic paraplegia 42  
hereditary spastic paraplegia 6  
hereditary spastic paraplegia 73  
hereditary spastic paraplegia 8  
Hernandez Fragoso Syndrome 
Holt-Oram syndrome  
hypomyelinating leukodystrophy 6  
hypophosphatasia +   
ichthyosis +   
ichthyosis vulgaris +   
Infectious Skin Diseases +   
iridogoniodysgenesis syndrome +   
juvenile polyposis syndrome +   
juvenile xanthogranuloma 
keratosis +   
Kimura disease 
LADD syndrome  
Larsen syndrome  
leg dermatosis 
LEOPARD syndrome +   
Li-Fraumeni syndrome +   
lipomatosis +   
localized scleroderma +   
Loeys-Dietz syndrome +   
loiasis 
Lynch syndrome +   
macrocephaly-autism syndrome  
Macroepiphyseal Dysplasia, McAlister Coe Type 
malignant hyperthermia +   
mandibulofacial dysostosis, Guion-Almeida type  
MASS Syndrome  
mastocytosis +   
maturity-onset diabetes of the young +   
McCune Albright syndrome  
Median Cleft Lip, Corpus Callosum, Lipoma, and Skin Polyps 
Mental Retardation, Joint Hypermobility, and Skin Laxity, with or without Metabolic Abnormalities 
Metabolic Skin Diseases +   
Microcephaly-Capillary Malformation Syndrome  
mitochondrial DNA depletion syndrome 12a  
mongolian spot 
monilethrix +   
Morgellons Disease 
Muckle-Wells syndrome  
multicentric reticulohistiocytosis 
multiple cutaneous and mucosal venous malformations  
An autosomal dominant disease that is characterized by multiple bluish cutaneous or mucosal venous lesions. (DO)
Multiple Endocrine Neoplasia +   
myofibrillar myopathy 1  
myofibrillar myopathy 2  
myofibrillar myopathy 4  
myofibrillar myopathy 5  
myofibrillar myopathy 6  
nail disease +   
nail-patella syndrome +   
necrobiosis lipoidica 
Necrobiotic Disorders +  
Necrolytic Migratory Erythema 
Nephrogenic Fibrosing Dermopathy  
neurofibromatosis +   
nevoid basal cell carcinoma syndrome +   
noninfectious dermatoses of eyelid +  
ocular albinism with sensorineural deafness  
Opitz GBBB Syndrome, Type II  
Opitz Trigonocephaly Syndrome  
otulipenia  
ovarian dysgenesis 8  
pachyonychia congenita +   
Pallister-Hall syndrome +   
Papulosquamous Skin Diseases +   
paraganglioma +   
Pelger-Huet anomaly +   
permanent neonatal diabetes mellitus +   
phaeohyphomycosis +  
phlebitis +   
photosensitive trichothiodystrophy +   
photosensitivity disease +   
piebaldism +   
pigmentation disease +   
polycystic liver disease +   
popliteal pterygium syndrome +   
portal vein thrombosis 
proximal symphalangism  
Prurigo  
Pruritus +   
Pseudoatrophoderma Colli 
pulmonary vein leiomyosarcoma 
punctate palmoplantar keratoderma type III 
Rapp-Hodgkin syndrome  
reactive cutaneous fibrous lesion +  
renal coloboma syndrome  
retinal vein occlusion +   
rosacea +   
Roy Maroteaux Kremp Syndrome 
Rubinstein-Taybi syndrome +   
SADDAN  
scalp dermatosis +   
sebaceous gland disease +   
Skin Abnormalities +   
skin atrophy 
Skin Neoplasms +   
skin sarcoidosis 
Spinal Arterial Venous Malformations with Cutaneous Hemangiomas 
spondyloepimetaphyseal dysplasia, Missouri type  
spondyloepimetaphyseal dysplasia, Strudwick type  
spondyloepiphyseal dysplasia congenita  
Stickler syndrome +   
strongyloidiasis  
superior vena cava angiosarcoma 
superior vena cava leiomyosarcoma 
sweat gland disease +   
systemic scleroderma +   
tarsal-carpal coalition syndrome  
Ter Haar Syndrome  
Tietz syndrome  
Timothy syndrome  
Townes-Brocks syndrome  
transthyretin amyloidosis  
Treacher Collins syndrome  
trichorhinophalangeal syndrome type I  
trichorhinophalangeal syndrome type II  
trichorhinophalangeal syndrome type III  
tuberous sclerosis +   
type 1 diabetes mellitus 2  
tyrosinemia type II  
Upton Young Syndrome 
urticaria +   
varicose veins +   
vascular skin disease +   
venous insufficiency +   
verruciform xanthoma of skin 
vesiculobullous skin disease +   
Waardenburg's syndrome +   

Synonyms
Exact Synonyms: Mucocutaneous Venous Malformations ;   VMCM ;   VMCM1
Primary IDs: MESH:C563977
Alternate IDs: OMIM:600195 ;   RDO:0013087
Definition Sources: http://ghr.nlm.nih.gov/condition/multiple-cutaneous-and-mucosal-venous-malformations, http://omim.org/entry/600195?search=600195&highlight=600195, https://www.ncbi.nlm.nih.gov/pubmed/20301733

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