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Term:
Sclerema Neonatorum (DOID:9002858)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0)
Parent Terms Term With Siblings Child Terms
acrodermatitis +   
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 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 
C1q Deficiency  
Caffey disease +   
Carney complex +   
Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal  
cocoon syndrome  
Colic 
Congenital Hyperinsulinism +   
congenital nystagmus +   
congenital syphilis +  
congenital toxoplasmosis 
Cutaneous Hemangiomatosis with Associated Features 
Cutis Laxa-Marfanoid Syndrome 
cystic fibrosis +   
Dermal Ridges, Nelson Syndrome 
Dermal Ridges, Patternless 
Dermoodontodysplasia 
dyskeratosis congenita +   
Dyskeratosis, Hereditary Benign Intraepithelial 
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 erythroblastosis +   
Hairy Palms and Soles 
hydrophthalmos +   
Hyperglycinemia, Transient Neonatal 
Hyperkeratotic Cutaneous Capillary-Venous Malformations Associated with Cerebral Capillary Malformations  
Hyperparathyroidism, Neonatal Severe Primary  
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  
Infantile Hypercalcemia +   
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma  
lethal restrictive dermopathy  
LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2  
LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 3  
meconium aspiration syndrome  
Meconium Ileus  
Michelin Tire Baby Syndrome +   
Microphthalmia, Syndromic 7  
Mobius syndrome +   
multiple pterygium syndrome +   
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 
Oculocerebrocutaneous Syndrome 
ophthalmia neonatorum 
PALMOPLANTAR CARCINOMA, MULTIPLE SELF-HEALING  
persistent fetal circulation syndrome  
poikiloderma with neutropenia  
Poikiloderma, Hereditary Sclerosing +   
Port-Wine Stain +   
Posttransfusion Purpura  
Premature Infant Diseases +   
Prolidase Deficiency  
pseudoxanthoma elasticum +   
Pterygium Colli, Isolated 
Ridges-off-the-end Syndrome 
Rothmund-Thomson syndrome +   
Sclerema Neonatorum 
A severe, sometimes fatal, disorder of adipose tissue occurring chiefly in preterm or debilitated infants suffering from an underlying illness and manifested by a diffuse, nonpitting induration of the affected tissue. The skin becomes cold, yellowish, mottled, and inflexible.
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, 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  
thanatophoric dysplasia +   
transient neonatal thrombocytopenia 
Trichothiodystrophy Syndromes +   
umbilical hernia +   
Urban Schosser Spohn Syndrome 
Vascular Hyalinosis 
vitamin K deficiency bleeding  
Winter Shortland Temple Syndrome  
Wolman disease +   
xeroderma pigmentosum +   

Synonyms
Primary IDs: MESH:D012593 ;   RDO:0006543
Definition Sources: MESH:D012593

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