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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
keratosis +     
Skin Abnormalities +     
acquired hyperkeratosis 
acrodermatitis +   
acrokeratosis verruciformis  
actinic keratosis +   
Amniotic Band Syndrome +  
Anetoderma +   
asphyxia neonatorum +   
Autoinflammation with Arthritis and Dyskeratosis  
Barber-Say syndrome  
Beare-Stevenson cutis gyrata syndrome  
benign neonatal seizures +   
Birth Injuries +   
Blepharophimosis with Ptosis, Syndactyly, and Short Stature 
blepharophimosis, ptosis, and epicanthus inversus syndrome +   
Bloch-Sulzberger syndrome +   
Book Syndrome 
C1q Deficiency +   
Caffey disease +   
Callosities +  
Carney complex +   
Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal  
cholesteatoma +   
Colic 
Congenital Hyperinsulinism +   
congenital nystagmus +   
congenital syphilis +  
congenital toxoplasmosis  
contractures, pterygia, and spondylocarpotarsal fusion syndrome +   
Curly Hair-Acral Keratoderma-Caries Syndrome 
Cutaneous Hemangiomatosis with Associated Features 
Cutis Laxa-Marfanoid Syndrome 
cystic fibrosis +   
Dermal Ridges, Nelson Syndrome 
Dermoodontodysplasia 
dyskeratosis congenita +   
ectodermal dysplasia +   
Ehlers-Danlos syndrome +   
epidermolysis bullosa +   
Epithelial Squamous Dysplasia, Keratinizing Desquamative, of Urinary Tract 
Erosive Arthropathy 
erythrokeratodermia variabilis +   
Familial Dyskeratotic Comedones 
Familial Popliteal Pterygium Syndrome 
fetal encasement syndrome  
Hairy Palms and Soles 
hemolytic disease of the fetus +   
Hereditary Benign Intraepithelial Dyskeratosis 
hereditary papulotranslucent acrokeratoderma 
Hereditary Sclerosing Poikiloderma +   
hydrophthalmos +   
Hyperkeratosis Lenticularis Perstans 
Hyperkeratotic Cutaneous Capillary-Venous Malformations Associated with Cerebral Capillary Malformations  
Hyperparathyroidism, Neonatal Severe Primary  
Hypohidrosis with Abnormal Palmar Dermal Ridges 
ichthyosis +   
A skin disease characterized by drying and scaling of skin with the accumulation of thick scales and cracks that may be painful or bleed. (DO)
Ichthyosis-Mental Retardation Syndrome with Large Keratohyalin Granules in the Skin 
Infantile Cataract, Skin Abnormalities, Glutamate Excess, and Impaired Intellectual Development  
Infantile Hypercalcemia +   
inflammatory poikiloderma with hair abnormalities and acral keratoses  
Isolated Pterygium Colli 
Johnston Aarons Schelley Syndrome 
Keratolytic Winter Erythema  
keratosis follicularis +   
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma  
meconium aspiration syndrome  
Meconium Ileus  
MLS syndrome +   
Moebius syndrome +   
multiple benign circumferential skin creases on limbs +   
Multiple Eruptive Milia 
Multiple Self-healing Palmoplantar Carcinoma  
neonatal abstinence syndrome  
Neonatal Alloimmune Thrombocytopenia  
neonatal anemia +   
neonatal diabetes +   
Neonatal Hyperbilirubinemia +   
Neonatal Hypoglycemia, Simulating Foetopathia Diabetica  
Neonatal Inflammatory Skin and Bowel Disease +   
Neonatal Pulmonary Hypertension  
Neonatal Sepsis  
Neurodevelopmental Disorder with Hypotonia, Dysmorphic Facies, and Skin Abnormalities  
Oculocerebrocutaneous Syndrome 
ophthalmia neonatorum 
palmoplantar keratosis +   
Parakeratosis  
Patternless Dermal Ridges 
persistent fetal circulation syndrome  
PLACK syndrome  
poikiloderma with neutropenia  
porokeratosis +   
Port-Wine Stain +   
Posttransfusion Purpura  
Premature Infant Diseases +   
prolidase deficiency  
pseudoxanthoma elasticum +   
restrictive dermopathy +   
Ridges-off-the-end Syndrome 
Rothmund-Thomson syndrome +   
Sclerema Neonatorum 
Sclerotylosis  
seborrheic keratosis +   
severe combined immunodeficiency +   
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  
thanatophoric dysplasia +   
Transient Neonatal Hyperglycinemia 
transient neonatal thrombocytopenia 
Trichostasis Spinulosa 
trichothiodystrophy +   
umbilical hernia +   
Urban Schosser Spohn Syndrome  
Vascular Hyalinosis 
vitamin K deficiency bleeding  
Winter Shortland Temple Syndrome  
Wolman disease +   
xeroderma pigmentosum +   
 IFAP Syndrome +   

Synonyms
Exact Synonyms: Ichthyoses ;   non-syndromic ichthyosis ;   xeroderma ;   xerodermas
Narrow Synonyms: Ichthyosis, ASPRV1-related
Primary IDs: MESH:D007057
Alternate IDs: OMIA:002099
Xrefs: MIM:PS146590 ;   NCI:C84776 ;   ORDO:79354
Definition Sources: http://purl.obolibrary.org/obo/HP_0008064 "DO" "DO", http://www.dermnetnz.org/topics/ichthyosis/ "DO" "DO", https://en.wikipedia.org/wiki/Ichthyosis "DO" "DO", https://www.ncbi.nlm.nih.gov/books/NBK1420/ "DO" "DO"

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