All individuals with variants in gene DAAM2

6 entries on 1 page. Showing entries 1 - 6.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00056297 - PubMed: Calvel 2015 2-generation family, affected boy and brother (different variants/phenotypes) F - Poland - - - - - ?, WDSTS 46,XY sexual development (DSD), complete gonadal dysgenes, Intrauterine growth retardation Postnatal growth retardation Short palpebral fissures Hypertelorism Epicanthus Wide nasal bridge/broad nasal tip Micrognathia Rib anomalies Delayed bone age Constipation Low hair line Developmental delay Intellectual disability Hypotonia Ambiguous genitalia Discordance between gender and karyotype Abnormal gonadal development Normal TSH, T4, GH, LH, high FSH, E2, low T levels 1 2 Guorui Hu
00056341 - PubMed: Calvel 2015 brother of 56297 M - Poland - - - - - ? penoscrotal hypospadias 1 1 Johan den Dunnen
00324103 B3174 PubMed: Schneider 2020, Journal: Schneider 2020 2-generation family, 1 affected, unaffected heterozygous carrier parents M no - Arab - - - - NPHS see paper; ..., steroid-resistant nephrotic syndrome 2 1 Johan den Dunnen
00324104 B1068 PubMed: Schneider 2020, Journal: Schneider 2020 - M yes - Arab - - - - NPHS see paper; ..., steroid-resistant nephrotic syndrome 1 1 Johan den Dunnen
00324105 HN-F629 PubMed: Schneider 2020, Journal: Schneider 2020 - M yes Turkey - - - - - NPHS see paper; ..., nephrotic syndrome 1 1 Johan den Dunnen
00324106 HN-F25 PubMed: Schneider 2020, Journal: Schneider 2020 - M yes - Arab - - - - NPHS see paper; ..., steroid-resistant nephrotic syndrome 1 1 Johan den Dunnen
Legend   How to query  


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