All individuals with variants in gene BMP7

21 entries on 1 page. Showing entries 1 - 21.
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00000208 - PubMed: Sun 2011, Journal: Sun 2011 - M no Netherlands - - - - - CHTE central hypothyroidism (FT4 0.50-0.99of lower limit normal), no prolactin deficiency, age sonographic determination testicular volume 17.64y, testicular volume right/left 21/20 (7.3–16ml) 1 1 Yu Sun
00204592 - PubMed: Wyatt 2010 - ? - - ? - - - - Healthy/Control - 1 1 LOVD
00204593 - PubMed: Wyatt 2010 - F - - ? - - - - ? Developmental Eye Anomalies. Right anophthalmia, haemangiomas upper eyelids, tracheooesophageal fistula, thoracic hemivertebrae, and intrauterine growth retardation. 1 1 LOVD
00204594 - PubMed: Wyatt 2010 - ? - - ? - - - - Healthy/Control - 1 1 LOVD
00204595 - PubMed: Wyatt 2010 - ? - - ? - - - - Healthy/Control - 1 1 LOVD
00204596 - PubMed: Wyatt 2010 - ? - - ? - - - - Healthy/Control - 1 1 LOVD
00204597 - PubMed: Wyatt 2010 - M - - ? - - - - ? Developmental Eye Anomalies. Bilateral anophthalmia, bilateral severe sensorineur hearing loss, high arched and cleft palate, axial hypotonia, scoliosis, developmental delay and seizure disorder. 1 1 LOVD
00204598 - PubMed: Wyatt 2010 Mother(carrier) has very high arched palate M - - ? - - - - ? Developmental Eye Anomalies. Unilateral microphthalmia, optic disc and chorioretinal coloboma. Mild learning difficulties. 1 1 LOVD
00204599 - PubMed: Wyatt 2010 - ? - - ? - - - - Healthy/Control - 1 1 LOVD
00204600 - PubMed: Wyatt 2010 - ? - - ? - - - - Healthy/Control - 1 1 LOVD
00204601 - PubMed: Wyatt 2010 - ? - - ? - - - - Healthy/Control - 1 1 LOVD
00204602 - PubMed: Wyatt 2010 - ? - - ? - - - - Healthy/Control - 1 1 LOVD
00204603 - PubMed: Wyatt 2010 - ? - - ? - - - - Healthy/Control - 1 1 LOVD
00204604 - PubMed: Wyatt 2010 Father (carrier) has a normal eye phenotype and other paternal relatives (grandmother and uncle of the proband) carrying the variant allele have no eye problems by report. F - - ? - - - - ? Developmental Eye Anomalies. Left microcornea with atypical iris coloboma, disorganised anterior segment, normal right eye with 20/20 vision, first finger malformation with split fingernail. 1 1 LOVD
00204605 - PubMed: Wyatt 2010 Father (carrier) has a normal eye phenotype and other paternal relatives (grandmother and uncle of the proband) carrying the variant allele have no eye problems by report. F - - ? - - - - ? Developmental Eye Anomalies. Left microcornea with atypical iris coloboma, disorganised anterior segment, normal right eye with 20/20 vision, first finger malformation with split fingernail. 1 1 LOVD
00204606 - PubMed: Wyatt 2010 Normal father ? - - ? - - - - ? Developmental Eye Anomalies. Two individuals with unilateral microphthalmia. 1 2 LOVD
00204607 - PubMed: Wyatt 2010 Parents of individual unavailable for testing. ? - - ? - - - - ? Developmental Eye Anomalies. Left iris coloboma, optic disc, and chorioretinal coloboma. 1 1 LOVD
00204608 - PubMed: Wyatt 2010 - ? - - ? - - - - Healthy/Control - 1 1 LOVD
00204609 - PubMed: Wyatt 2010 - ? - - ? - - - - Healthy/Control - 1 1 LOVD
00326949 MRK444 PubMed: Chen 2021, Journal: Chen 2021 - F - China Han - - - - MRKHS see paper; ... 1 1 Johan den Dunnen
00326950 MRK342 PubMed: Chen 2021, Journal: Chen 2021 - F - China Han - - - - MRKHS see paper; ... 1 1 Johan den Dunnen
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