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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
keratosis +     
Skin Abnormalities +     
skin disease +     
Achenbach syndrome 
Acneiform Eruptions +   
acquired hyperkeratosis 
acrodermatitis +   
acrokeratosis verruciformis  
actinic keratosis +   
adiaspiromycosis 
allergic cutaneous vasculitis +   
Amniotic Band Syndrome +  
ancylostomiasis +  
Anetoderma +   
angioedema +   
asphyxia neonatorum +   
AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS  
Barber-Say syndrome  
Beare-Stevenson cutis gyrata syndrome  
benign neonatal seizures +   
Birth Injuries +   
Blepharophimosis Syndrome Type 1  
Blepharophimosis Syndrome Type 2  
Blepharophimosis with Ptosis, Syndactyly, and Short Stature 
blepharophimosis, ptosis, and epicanthus inversus syndrome  
Bloch-Sulzberger syndrome +   
Book Syndrome 
Boudhina Yedes Khiari syndrome 
breast disease +   
C1q Deficiency  
Caffey disease +   
Callosities +  
Carney complex +   
Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal  
cercarial dermatitis 
chancroid +  
cholesteatoma +   
chronic ulcer of skin +   
cocoon syndrome  
coenurosis 
Colic 
Congenital Hyperinsulinism +   
congenital nystagmus +   
congenital syphilis +  
congenital toxoplasmosis 
contagious pustular dermatitis 
Curly Hair-Acral Keratoderma-Caries Syndrome 
Cutaneous Fistula 
Cutaneous Hemangiomatosis with Associated Features 
cutaneous lupus erythematosus +   
cutis laxa +   
Cutis Laxa-Marfanoid Syndrome 
cystic fibrosis +   
Dermal Fibrosis  
Dermal Ridges, Nelson Syndrome 
Dermal Ridges, Patternless 
dermatitis +   
Dermatoleukodystrophy 
dermatomyositis +   
Dermoodontodysplasia 
dipetalonemiasis 
Duplication of Eyebrows with Stretchable Skin and Syndactyly 
dyskeratosis congenita +   
Dyskeratosis, Hereditary Benign Intraepithelial 
ectodermal dysplasia +   
Ectodermal Dysplasia-Skin Fragility Syndrome  
Eczematous Skin Diseases +   
Ehlers-Danlos syndrome +   
Elastosis Perforans Serpiginosa 
Elliott Ludman Teebi Syndrome 
endometriosis in scar of skin 
epidermal nevus +   
epidermolysis bullosa +   
epidermolytic hyperkeratosis +   
Epithelial Squamous Dysplasia, Keratinizing Desquamative, of Urinary Tract 
Erosive Arthropathy 
Erythema +   
erythematosquamous dermatosis 
erythrokeratodermia variabilis +   
exanthem +   
FACES Syndrome 
facial dermatosis +   
Facial Ectodermal Dysplasia  
Familial Dyskeratotic Comedones 
Familial Popliteal Pterygium Syndrome 
fetal erythroblastosis +   
filariasis +   
Flynn Aird Syndrome 
Focal Facial Dermal Dysplasia 4  
Foot Diseases +   
Genetic Skin Diseases +   
granulomatosis with polyangiitis +   
hair disease +   
Hairy Palms and Soles 
hand dermatosis +  
hemorrhoid +   
hereditary papulotranslucent acrokeratoderma 
Hernandez Fragoso Syndrome 
hydrophthalmos +   
Hyperglycinemia, Transient Neonatal 
Hyperkeratosis Lenticularis Perstans 
Hyperkeratotic Cutaneous Capillary-Venous Malformations Associated with Cerebral Capillary Malformations  
Hyperparathyroidism, Neonatal Severe Primary  
Hypohidrosis with Abnormal Palmar Dermal Ridges 
ichthyosis +   
Any of several generalized skin disorders characterized by dryness, roughness, and scaliness, due to hypertrophy of the stratum corneum epidermis. Most are genetic, but some are acquired, developing in association with other systemic disease or genetic syndrome.
Ichthyosis-Mental Retardation Syndrome with Large Keratohyalin Granules in the Skin 
Infantile Cataract, Skin Abnormalities, Glutamate Excess, and Impaired Intellectual Development  
Infantile Hypercalcemia +   
Infectious Skin Diseases +   
Johnston Aarons Schelley Syndrome 
juvenile xanthogranuloma 
Keratolytic Winter Erythema  
keratosis +   
keratosis follicularis +   
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma  
Kimura disease 
leg dermatosis 
lethal restrictive dermopathy  
LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2  
LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 3  
lipomatosis +   
localized scleroderma +   
loiasis 
Macroepiphyseal Dysplasia, McAlister Coe Type 
MASS Syndrome  
mastocytosis +   
meconium aspiration syndrome  
Meconium Ileus  
Median Cleft Lip, Corpus Callosum, Lipoma, and Skin Polyps 
Mental Retardation, Joint Hypermobility, and Skin Laxity, with or without Metabolic Abnormalities 
Metabolic Skin Diseases +   
Michelin Tire Baby Syndrome +   
Microphthalmia, Syndromic 7  
Mobius syndrome +   
mongolian spot 
Morgellons Disease 
multicentric reticulohistiocytosis 
multiple cutaneous and mucosal venous malformations  
Multiple Eruptive Milia 
multiple pterygium syndrome +   
nail disease +   
necrobiosis lipoidica 
Necrobiotic Disorders +  
Necrolytic Migratory Erythema 
neonatal abstinence syndrome 
Neonatal Alloimmune Thrombocytopenia  
neonatal anemia +   
neonatal diabetes mellitus +   
Neonatal Hyperbilirubinemia +   
Neonatal Hypoglycemia, Simulating Foetopathia Diabetica 
Neonatal Inflammatory Skin and Bowel Disease +   
Neonatal Pulmonary Hypertension  
Neonatal Sepsis 
Nephrogenic Fibrosing Dermopathy  
noninfectious dermatoses of eyelid +  
Oculocerebrocutaneous Syndrome 
ophthalmia neonatorum 
Opitz Trigonocephaly Syndrome  
otulipenia  
PALMOPLANTAR CARCINOMA, MULTIPLE SELF-HEALING  
palmoplantar keratosis +   
Papulosquamous Skin Diseases +   
Parakeratosis  
PEELING SKIN WITH LEUKONYCHIA, ACRAL PUNCTATE KERATOSES, CHEILITIS, AND KNUCKLE PADS  
persistent fetal circulation syndrome  
phaeohyphomycosis +  
photosensitivity disease +   
pigmentation disease +   
poikiloderma with neutropenia  
Poikiloderma, Hereditary Sclerosing +   
porokeratosis +   
Port-Wine Stain +   
Posttransfusion Purpura  
Premature Infant Diseases +   
Prolidase Deficiency  
Prurigo  
Pruritus +   
Pseudoatrophoderma Colli 
pseudoxanthoma elasticum +   
Pterygium Colli, Isolated 
reactive cutaneous fibrous lesion +  
Ridges-off-the-end Syndrome 
rosacea +   
Rothmund-Thomson syndrome +   
Roy Maroteaux Kremp Syndrome 
scalp dermatosis +   
Sclerema Neonatorum 
Sclerotylosis 
sebaceous gland disease +   
seborrheic keratosis +   
severe combined immunodeficiency +   
Skin Abnormalities +   
skin atrophy 
Skin Neoplasms +   
skin sarcoidosis 
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, 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  
Skin/Hair/Eye Pigmentation, Variation In, 9  
strongyloidiasis  
sweat gland disease +   
systemic scleroderma +   
Ter Haar Syndrome  
thanatophoric dysplasia +   
transient neonatal thrombocytopenia 
Trichostasis Spinulosa 
Trichothiodystrophy Syndromes +   
tyrosinemia type II  
umbilical hernia +   
Upton Young Syndrome 
Urban Schosser Spohn Syndrome 
urticaria +   
Vascular Hyalinosis 
vascular skin disease +   
verruciform xanthoma of skin 
vesiculobullous skin disease +   
vitamin K deficiency bleeding  
Winter Shortland Temple Syndrome  
Wolman disease +   
xeroderma pigmentosum +   

Synonyms
Exact Synonyms: Ichthyoses ;   Xeroderma ;   Xerodermas ;   non-syndromic ichthyosis
Narrow Synonyms: Ichthyosis, ASPRV1-related
Primary IDs: MESH:D007057 ;   RDO:0001008
Alternate IDs: OMIA:002099
Xrefs: ORDO:79354
Definition Sources: MESH:D007057, http://purl.obolibrary.org/obo/HP_0008064, http://www.dermnetnz.org/topics/ichthyosis/, https://en.wikipedia.org/wiki/Ichthyosis, https://www.ncbi.nlm.nih.gov/books/NBK1420/

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