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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Rare genetic hepatic disease +     
skin disease +     
Achenbach syndrome 
Acute infantile liver failure-multisystemic involvement syndrome 
Alopecia - epilepsy - pyorrhea - intellectual disability 
Alopecia - intellectual disability - hypergonadotropic hypogonadism 
alopecia areata  
Alopecia universalis 
Alopecia-intellectual disability syndrome 
Alternariosis 
androgenetic alopecia +   
Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema 
Bazex-Dupre-Christol syndrome +  
chemotherapy-induced alopecia  
chloracne 
Cholestasis-lymphedema syndrome 
Lymphedema cholestasis syndrome (LCS) is a rare genetic disorder characterized by neonatal intrahepatic cholestasis, often lessening and becoming intermittent with age, and severe chronic lymphedema which mainly affects the lower limbs. Patients often present fat malabsorption leading to failure to thrive, fat soluble vitamin deficiency with bleeding, rickets, neuropathy. In 25% of cases, cirrhosis occurs, during childhood or later in life.
cicatricial alopecia 
congenital lethal erythroderma 
cutaneous mucinosis +  
Deafness - lymphedema - leukemia 
dermatitis +   
dermatological toxicity  
dermis disorder +   
diabetic foot  
edema  
epidermal disease +   
erythema multiforme 
erythema palmare hereditarium 
erythematosquamous dermatosis  
exanthem +   
facial dermatosis +  
hand dermatosis 
Hand-foot syndrome  
Hepatic fibrosis - renal cysts - intellectual disability 
Hepatic veno-occlusive disease - immunodeficiency 
hereditary epidermal appendage anomaly +   
hereditary skin disorder +   
hyperglobulinemic purpura 
Hypotrichosis - lymphedema - telangiectasia 
Ichthyosis-hypotrichosis syndrome 
inflammatory skin disease +   
Isolated polycystic liver disease 
keratosis +   
keratosis pilaris +  
Kimura disease 
Late-onset primary lymphedema +  
leg dermatosis 
lichen disease +   
lipodystrophy +  
Lissencephaly syndrome, Norman-Roberts type 
Livedo reticularis 
Lymphedema - atrial septal defects - facial changes 
Lymphedema - cerebral arteriovenous anomaly 
Lymphedema - cleft palate 
Lymphedema - distichiasis 
lymphedema, hereditary, iii 
maculopapular eruption  
Milroy disease 
mongolian spot 
multiple benign circumferential skin creases on limbs +  
Müllerian derivatives - lymphangiectasia - polydactyly 
Necrobiotic Xanthogranuloma 
neonatal erythema toxicum 
nephrogenic fibrosing dermopathy 
nevus +   
non-neoplastic nevus  
panniculitis +  
Parana hard-skin syndrome 
paronychia +  
PEHO-like syndrome 
pigmentation disease +   
prurigo nodularis  
Pyoderma gangrenosum-acne-suppurative hidradenitis syndrome 
Rare metabolic liver disease +   
reactive cutaneous fibrous lesion +   
rosacea  
scalp dermatosis 
Scarring alopecia of scalp 
sebaceous gland disease +   
severe cutaneous adverse reaction +   
skin atrophy 
skin disorder caused by infection +   
skin neoplasm +   
skin pigmentation disorder +  
skin reaction 
skin sarcoidosis 
skin vascular disease +   
sunburn  
susceptibility to malaria 
sweat gland disease +   
Syndromic diarrhea 
systemic scleroderma +   
toxic dermatosis +   
vesiculobullous skin disease +   
Yellow Nail Syndrome 

Synonyms
Exact Synonyms: Aagenaes syndrome
Xrefs: ICD10:Q82.0 ;   MIM:214900

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