Phenotypes for disease #03964 (ILLD (lung and liver disease, interstitial (ILLD, liver failure syndrome, infantile, type 2)), OMIM:615486)

7 entries on 1 page. Showing entries 1 - 7.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000059090 Failure to thrive; Interstitial lung disease; Steatosis; Fibrosis; Cholestasis; Bridging necrosis; Hemosiderin-laden macrophages in the portal tract; Vomit; Hypothyroidism; Anemia; Arrest of RBC mature; Thrombocytosis; Abnormal liver enzymes; Aminoaciduria; Lactic acidosis, intermittent; - - Familial, autosomal recessive - - - - - Guorui Hu 00079366
0000059091 see paper; ... - - Familial, autosomal recessive - - - - - Guorui Hu 00079367
0000068566 see paper; ... - - Familial, autosomal recessive - - - - - Johan den Dunnen 00089179
0000068568 failure to thrive 22/29; respiratory insufficiency 14/29; dyspnea 28/29; cough 7/29; interstitial lung disease; lung fibrosis 12/18; hepatomegaly 25/28; liver dysfunction 24/28; steatosis 5/28; fibrosis 1/28; cirrhosis 8/28; digital clubbing 8/29 - - Familial, autosomal recessive - - - - - Guorui Hu 00089181
0000068569 see paper; ... - - Familial, autosomal recessive - - - - - Johan den Dunnen 00089182
0000068574 - - - Familial, autosomal recessive - - - - - Guorui Hu 00079370
0000125986 HP:0006530 HP:0000821 HP:0001903 HP:0002093 - - Familial, autosomal recessive - - - - - Tamar Harel 00153305
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