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| Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic v0.161 | Bryony Thompson Copied STR HOXA13_HFGS_GCN3 from panel Repeat Disorders | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic v0.161 | HOXA13_HFGS_GCN3 |
Bryony Thompson STR: HOXA13_HFGS_GCN3 was added STR: HOXA13_HFGS_GCN3 was added to Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic. Sources: Expert Review Green,Expert list paediatric-onset tags were added to STR: HOXA13_HFGS_GCN3. Mode of inheritance for STR: HOXA13_HFGS_GCN3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for STR: HOXA13_HFGS_GCN3 were set to 10839976; 12073020; 33811808 Phenotypes for STR: HOXA13_HFGS_GCN3 were set to Hand-foot-uterus syndrome MIM#140000 |
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| Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic v0.0 | HOXA13 |
Zornitza Stark gene: HOXA13 was added gene: HOXA13 was added to Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: HOXA13 was set to Unknown |
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