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Term:
ichthyosis vulgaris (DOID:1702)
Annotations: Rat: (2) Mouse: (2) Human: (3) Chinchilla: (1) Bonobo: (2) Dog: (2) Squirrel: (1)
Parent Terms Term With Siblings Child Terms
ichthyosis +     
abdominal obesity-metabolic syndrome +   
ablepharon macrostomia syndrome  
Absence of Fingerprints  
achondrogenesis type II  
Acquired Ichthyosis 
acrofacial dysostosis Cincinnati type  
acrokeratosis verruciformis  
Actinic Prurigo  
ADULT syndrome  
adult-onset autosomal dominant demyelinating leukodystrophy  
advanced sleep phase syndrome +   
age related macular degeneration +   
Albinism +   
Alexander Disease  
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  
Andersen-Tawil syndrome  
ankyloblepharon-ectodermal defects-cleft lip/palate syndrome  
Annular Erythema 
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  
arterial tortuosity syndrome  
atopic dermatitis +   
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  
Atrophia Maculosa Varioliformis Cutis, Familial 
autoimmune lymphoproliferative syndrome type 2A  
autoimmune lymphoproliferative syndrome type 4  
AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS  
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 +   
autosomal recessive congenital ichthyosis +   
Axenfeld-Rieger syndrome +   
Bannayan-Riley-Ruvalcaba syndrome  
Bart-Pumphrey syndrome  
Basaloid Follicular Hamartoma Syndrome, Generalized, Autosomal Dominant 
Beare-Stevenson cutis gyrata syndrome  
Birk-Barel syndrome  
Birt-Hogg-Dube syndrome  
Blau syndrome  
blepharocheilodontic syndrome +   
blepharophimosis, ptosis, and epicanthus inversus syndrome  
Bloch-Sulzberger syndrome +   
blue color blindness  
brachydactyly type A1 +   
brachydactyly type A2  
brachydactyly type C  
brachydactyly type D  
branchiooculofacial syndrome  
branchiootorenal syndrome +   
Brooke-Spiegler syndrome  
Brown-Vialetto-Van Laere syndrome +   
Brugada syndrome 1  
Brugada syndrome 7  
Brugada syndrome 9  
bullous congenital ichthyosiform erythroderma  
Buschke-Ollendorff Syndrome  
CADASIL 1  
CADASIL 2  
campomelic dysplasia +   
Camptodactyly-Ichthyosis Syndrome 
Carney complex +   
Cataract and Congenital Ichthyosis 
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 +   
Clouston syndrome  
Collagenosis, Familial Reactive Perforating 
Congenital Erythroderma with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-IgE  
Congenital Ichthyosis with Trichothiodystrophy +   
Costello syndrome  
Cowden syndrome +   
Crouzon syndrome-acanthosis nigricans syndrome  
Culler-Jones syndrome  
Cutaneous Bullous Amyloidosis 
cutaneous porphyria  
cutis laxa +   
Deal Barratt Dillon Syndrome 
Denys-Drash syndrome  
Dowling-Degos disease +   
Duane-radial ray syndrome  
Dykes Markes Harper Syndrome 
dyschromatosis universalis hereditaria +   
dyskeratosis congenita +   
dysplastic nevus syndrome +   
ectodermal dysplasia +   
EEC syndrome +   
Ehlers-Danlos syndrome +   
epidermolysis bullosa +   
erythrokeratodermia variabilis +   
Erythrokeratodermia with Ataxia  
Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-like  
familial cold autoinflammatory syndrome 4  
familial erythrocytosis 1  
familial erythrocytosis 3  
familial erythrocytosis 5  
Feingold syndrome +   
Follicular Atrophoderma, Perioral Pigmented, with Milia and Epidermoid Cysts 
Frasier syndrome  
Gerodermia Osteodysplastica  
Grover's Disease 
Hailey-Hailey disease  
Hajdu-Cheney syndrome  
hand-foot-genital syndrome  
Hepatic Porphyrias +   
Hereditary Autoinflammatory Diseases +   
hereditary breast ovarian cancer syndrome +   
hereditary hemorrhagic telangiectasia +   
hereditary mucosal leukokeratosis  
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  
HID Syndrome  
Histiocytic Dermatoarthritis 
Holt-Oram syndrome  
Hyaluronan Metabolism, Defect in 
hypomyelinating leukodystrophy 6  
hypophosphatasia +   
Ichthyosis Cheek Eyebrow Syndrome 
Ichthyosis Exfoliativa  
Ichthyosis Follicularis Atrichia Photophobia Syndrome  
Ichthyosis Hystrix Gravior 
Ichthyosis Hystrix, Curth Macklin Type  
Ichthyosis Prematurity Syndrome  
Ichthyosis Tapered Fingers Midline Groove Up 
ichthyosis vulgaris +   
Most common form of ICHTHYOSIS characterized by prominent scaling especially on the exterior surfaces of the extremities. It is inherited as an autosomal dominant trait.
Ichthyosis, Mental Retardation, Dwarfism, and Renal Impairment 
Ichthyosis, Spastic Quadriplegia, and Mental Retardation  
Ichthyosis, Split Hairs, and Amino Aciduria 
Ichthyosis-Mental Retardation Syndrome with Large Keratohyalin Granules in the Skin 
iridogoniodysgenesis syndrome +   
Isolated Osteopoikilosis 
Jagell Holmgren Hofer Syndrome 
juvenile polyposis syndrome +   
Juvenile Spring Eruption of Ears 
Keratolytic Winter Erythema  
keratosis follicularis +   
Keratosis Follicularis Spinulosa Decalvans, X-Linked  
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma  
Koone Rizzo Elias Syndrome 
LADD syndrome  
Larsen syndrome  
LEOPARD syndrome +   
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
Li-Fraumeni syndrome +   
lipoid proteinosis  
Loeys-Dietz syndrome +   
Lynch syndrome +   
macrocephaly-autism syndrome  
malignant hyperthermia +   
mandibulofacial dysostosis, Guion-Almeida type  
maturity-onset diabetes of the young +   
McCune Albright syndrome  
mitochondrial DNA depletion syndrome 12a  
monilethrix +   
Muckle-Wells syndrome  
Muir-Torre syndrome  
multiple cutaneous and mucosal venous malformations  
Multiple Endocrine Neoplasia +   
Multiple Noduli Cutanei with Urinary Tract Abnormalities 
myofibrillar myopathy 1  
myofibrillar myopathy 2  
myofibrillar myopathy 4  
myofibrillar myopathy 5  
myofibrillar myopathy 6  
nail-patella syndrome +   
Neu-Laxova syndrome 1  
neurofibromatosis +   
nevoid basal cell carcinoma syndrome +   
Nisch syndrome  
ocular albinism with sensorineural deafness  
Oculotrichodysplasia 
Opitz GBBB Syndrome, Type II  
orofaciodigital syndrome IX  
Osteosclerosis with Ichthyosis and Fractures 
ovarian dysgenesis 8  
pachyonychia congenita +   
Pallister-Hall syndrome +   
palmoplantar keratosis +   
paraganglioma +   
Parana Hard Skin Syndrome 
Pedal Onychogryposis with Keratosis Plantaris and Coarse Hair 
peeling skin syndrome +   
Pelger-Huet anomaly +   
Perifolliculitis Capitis Abscedens Et Suffodiens, Familial 
permanent neonatal diabetes mellitus +   
photosensitive trichothiodystrophy +   
piebaldism +   
Plasminogen Deficiency, Type I  
Poikiloderma, Hereditary Sclerosing +   
polycystic liver disease +   
popliteal pterygium syndrome +   
porokeratosis +   
primary cutaneous amyloidosis  
Primary Localized Cutaneous Amyloidosis, 2  
Primary Localized Cutaneous Amyloidosis, 3  
Progressive Osseous Heteroplasia  
Progressive Vitiligo with Mental Retardation and Urethral Duplication 
Prolidase Deficiency  
proximal symphalangism  
pseudoxanthoma elasticum +   
punctate palmoplantar keratoderma type III 
Rapp-Hodgkin syndrome  
renal coloboma syndrome  
Reticulate Pigmentary Disorder, with Systemic Manifestations  
Rothmund-Thomson syndrome +   
Rubinstein-Taybi syndrome +   
Rud Syndrome 
Ruzicka Goerz Anton syndrome 
SADDAN  
Sammartino De Crecchio Syndrome 
Sjogren-Larsson syndrome +   
Skin Fragility-Woolly Hair Syndrome  
spondyloepimetaphyseal dysplasia, Missouri type  
spondyloepimetaphyseal dysplasia, Strudwick type  
spondyloepiphyseal dysplasia congenita  
Stickler syndrome +   
Stiff Skin Syndrome  
Storm Syndrome 
Stormorken syndrome  
Systemic Hyalinosis  
tarsal-carpal coalition syndrome  
Tietz syndrome  
Timothy syndrome  
Townes-Brocks syndrome  
transthyretin amyloidosis  
Treacher Collins syndrome  
Trichodysplasia-Xeroderma 
trichorhinophalangeal syndrome type I  
trichorhinophalangeal syndrome type II  
trichorhinophalangeal syndrome type III  
Trichothiodystrophy Syndromes +   
tuberous sclerosis +   
type 1 diabetes mellitus 2  
Vohwinkel Syndrome, Variant Form  
Waardenburg's syndrome +   
X-linked ichthyosis +   
xeroderma of eyelid 
xeroderma pigmentosum +   
Zunich Neuroectodermal Syndrome  

Synonyms
Exact Synonyms: Ichthyosis Simplex ;   dominant congenital ichthyosiform erythroderma ;   dominant ichthyosis vulgaris ;   ichthyosis simplices
Primary IDs: MESH:D016112
Alternate IDs: OMIM:146700 ;   RDO:0000129
Xrefs: GARD:6752
Definition Sources: MESH:D016112, https://www.mayoclinic.org/diseases-conditions/ichthyosis-vulgaris/symptoms-causes/syc-20373754

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