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Ontology Browser

Term:
Hyperkeratotic Cutaneous Capillary-Venous Malformations Associated with Cerebral Capillary Malformations (DOID:9002924)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1) Naked Mole-rat: (1) Green Monkey: (1)
Parent Terms Term With Siblings Child Terms
acrodermatitis +   
Anetoderma +   
arteriovenous malformations of the brain +   
Autoinflammation with Arthritis and Dyskeratosis  
Barber-Say syndrome  
Beare-Stevenson cutis gyrata syndrome  
Blepharophimosis with Ptosis, Syndactyly, and Short Stature 
blepharophimosis, ptosis, and epicanthus inversus syndrome +   
Bloch-Sulzberger syndrome +   
Book Syndrome 
C1q Deficiency +   
Carney complex +   
Cavernous Malformations of CNS and Retina  
Central Nervous System Venous Angioma  
cerebral cavernous malformation +   
contractures, pterygia, and spondylocarpotarsal fusion syndrome +   
Cutaneous Hemangiomatosis with Associated Features 
Dermal Ridges, Nelson Syndrome 
Dermoodontodysplasia 
dyskeratosis congenita +   
ectodermal dysplasia +   
Ehlers-Danlos syndrome +   
epidermolysis bullosa +   
Epithelial Squamous Dysplasia, Keratinizing Desquamative, of Urinary Tract 
Erosive Arthropathy 
Familial Dyskeratotic Comedones 
Familial Popliteal Pterygium Syndrome 
fetal encasement syndrome  
Hairy Palms and Soles 
Hereditary Benign Intraepithelial Dyskeratosis 
Hereditary Sclerosing Poikiloderma +   
Hyperkeratotic Cutaneous Capillary-Venous Malformations Associated with Cerebral Capillary Malformations  
Hypohidrosis with Abnormal Palmar Dermal Ridges 
ichthyosis +   
Ichthyosis-Mental Retardation Syndrome with Large Keratohyalin Granules in the Skin 
Infantile Cataract, Skin Abnormalities, Glutamate Excess, and Impaired Intellectual Development  
inflammatory poikiloderma with hair abnormalities and acral keratoses  
Isolated Pterygium Colli 
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma  
MLS syndrome +   
multiple benign circumferential skin creases on limbs +   
Multiple Self-healing Palmoplantar Carcinoma  
Neurodevelopmental Disorder with Hypotonia, Dysmorphic Facies, and Skin Abnormalities  
Oculocerebrocutaneous Syndrome 
Patternless Dermal Ridges 
poikiloderma with neutropenia  
Port-Wine Stain +   
prolidase deficiency  
pseudoxanthoma elasticum +   
restrictive dermopathy +   
Ridges-off-the-end Syndrome 
Rothmund-Thomson syndrome +   
Sclerema Neonatorum 
Sinus Pericranii 
Skin/Hair/Eye Pigmentation, Variation In, 1  
Skin/Hair/Eye Pigmentation, Variation In, 10  
Skin/Hair/Eye Pigmentation, Variation In, 11  
SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 2  
Skin/Hair/Eye Pigmentation, Variation In, 3  
Skin/Hair/Eye Pigmentation, Variation In, 4  
Skin/Hair/Eye Pigmentation, Variation In, 5  
Skin/Hair/Eye Pigmentation, Variation In, 6  
Skin/Hair/Eye Pigmentation, Variation In, 7  
Skin/Hair/Eye Pigmentation, Variation In, 8  
trichothiodystrophy +   
Urban Schosser Spohn Syndrome  
Vascular Hyalinosis 
Winter Shortland Temple Syndrome  
xeroderma pigmentosum +   

Synonyms
Primary IDs: MESH:C566153

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