Phenotypes for disease #03803 (CHTD2 (heart defects, congenital, nonsyndromic, type 2 (CHTD2), OMIM:614980)

2 entries on 1 page. Showing entries 1 - 2.
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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     
0000272435 cardiovascular anomalies, recurrent facial dysmorphisms, generalized joint hypermobility and soft/velvetyhyperextensible skin - TAB2 multisystem disorder with cardiovascular, cutaneous, musculoskeletal and facial involvement Unknown 05y - - - - Cecilia Giunta 00377280
0000272448 cardiomyopathy,dilated aortic dissection type B inguinal hernia hypospadias multicystic kindney gastro-intestinal malrotation conductive hearing loss short stature facial dysmorphism (ptosis, hypotelorism) prostate cancer - - Unknown 59y 59y - - - Jeroen Breckpot 00377296
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