Phenotypes for disease #01604 (WS1 (Waardenburg syndrome, type 1 (WS1)), OMIM:193500)

10 entries on 1 page. Showing entries 1 - 10.
Legend   How to query  

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000078850 - - - Unknown - - - - - Johan den Dunnen 00100622
0000257299 Heterochromia iris, telecanthus, white forelock, bilateral profound to severe hearing loss and hypopigmented patches of skin on the forehead, chest and upper limbs. Father (II-2) and paternal grandmother (I-2) had heterochromis irides. Mother (II-3) had white forelock - - Familial, autosomal dominant - - - - - Anju Shukla 00361903
0000272128 - - - Familial, autosomal dominant - - - - - Karina Lezirovitz Mandelbaum 00376927
0000272131 - - - Familial, autosomal dominant - - - - - Karina Lezirovitz Mandelbaum 00376929
0000272133 - - - Familial, autosomal dominant - - - - - Karina Lezirovitz Mandelbaum 00376932
0000274566 - - - Familial, autosomal dominant - - - - - Karina Lezirovitz Mandelbaum 00380713
0000274567 - - - Familial, autosomal dominant - - - - - Karina Lezirovitz Mandelbaum 00380714
0000274568 - - - Familial, autosomal dominant - - - - - Karina Lezirovitz Mandelbaum 00380715
0000275380 normal hearing, Partial heterochromia irides and white hair forelock, Telecanthus, high palate, cupid arc mouth, nasal wings hypoplasia, nasal root hyperplasia, and synophris - - Familial, autosomal dominant - - - - - Karina Lezirovitz Mandelbaum 00381530
0000275381 normal hearing, iris heterocromia, telecanthus, white hair forelock, synophris - - Familial, autosomal dominant - - - - - Karina Lezirovitz Mandelbaum 00381531
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.