All individuals with variants in gene MAX

21 entries on 1 page. Showing entries 1 - 21.
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00103834 21685915-FamCPat924 PubMed: Comino-Méndez 2011 3-generation family, affected brother/sister F no Italy white - - - - pheochromocytoma bilateral adrenal pheochromocytoma; malignant; Unkown familial antecedents; Tumor 2nd hit: uniparental disomy; Exclusive paternal MEG3 allele detection 1 2 Alberto Cascon
00103835 21685915-FamCPat922 PubMed: Comino-Méndez 2011 - M no - - - - - - pheochromocytoma Non-malignant 1 1 Alberto Cascon
00103836 21685915-FamDPat190 PubMed: Comino-Méndez 2011 - M - - - - - - - pheochromocytoma bilateral adrenal pheochromocytoma; non-malignant; No familial antecedents; Tumor 2nd hit: 14q loss; exclusive paternal MEG3 allele detection 1 1 Alberto Cascon
00103837 21685915-FamFPat368 PubMed: Comino-Méndez 2011 no familial antecedents F - - - - - - - pheochromocytoma Malignant 1 1 Alberto Cascon
00103838 21685915-FamAPat3121 PubMed: Comino-Méndez 2011 3-generation family, 4 affecteds (2F, 2M) M - - - - - - - pheochromocytoma bilateral adrenal pheochromocytoma; non-malignant 1 4 Alberto Cascon
00103839 21685915-FamAPat3119 PubMed: Comino-Méndez 2011 - M - - - - - - - pheochromocytoma bilateral adrenal pheochromocytoma; non-malignant 1 1 Alberto Cascon
00103840 21685915-FamAPat1090 PubMed: Comino-Méndez 2011 - F - - - - - - - pheochromocytoma bilateral adrenal pheochromocytoma; non-malignant 1 1 Alberto Cascon
00103841 21685915-FamAPat3122 PubMed: Comino-Méndez 2011 - F - - - - - - - pheochromocytoma bilateral adrenal pheochromocytoma; non-malignant 1 1 Alberto Cascon
00103842 21685915-FamEPat1016 PubMed: Comino-Méndez 2011 - F - - - - - - - pheochromocytoma bilateral adrenal pheochromocytoma; non-malignant; Paternal familial antecedents; Tumor 2nd hit: 14q loss; Exclusive paternal MEG3 allele detection 1 1 Alberto Cascon
00103843 21685915-FamHPatF31S PubMed: Comino-Méndez 2011 - F - - - - - - - pheochromocytoma Non-malignant; Paternal familial antecedents; Tumor 2nd hit; uniparental disomy; exclusive paternal MEG3 allele detection 1 1 Alberto Cascon
00103844 21685915-FamB PubMed: Comino-Méndez 2011 - M - - - - - - - pheochromocytoma bilateral adrenal pheochromocytoma; malignant 1 1 Alberto Cascon
00103845 21685915-FamG PubMed: Comino-Méndez 2011 no familial antecedents F - - - - - - - pheochromocytoma Non-malignant 1 1 Alberto Cascon
00264002 - - - F - - - - - - - MINAS Phaeochromocytoma, 16y; Phaeochromocytoma, 35y. 1 1 James Whitworth
00291093 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00296671 - - - F - - - - - - - ? Pheochromocytoma (HP:0002666); Hypertension (HP:0000822) 1 1 Andreas Laner
00372031 4067 - - M - (Italy) Asian - - yes - pheochromocytoma - 1 1 Luigi Mori
00396860 - PubMed: Kim 2021 - - - Korea - - - - - ? - 1 1 Johan den Dunnen
00445144 Pat1 PubMed: Harris 2024, Journal: Harris 2024 2-generation family, 1 affected, unaffected non-carrier parents M - United Kingdom (Great Britain) - - - - - ? see paper; .., macrocephaly, 0y0m-OFC 1.94, 7y1m-OFC +3.4; ventriculomegaly; polydactyly; intellectual disability appropriate for level of visual impairment; autistic traits; chorio-retinal colobomas affecting optic nerves and vision; developed exudative retinopathy in both eyes; persistent patent foramen ovale (now closed); gastro-esophageal reflux, 4 phalanges on left thumb, pectus carinatum 1 1 Johan den Dunnen
00445145 Pat2 PubMed: Harris 2024, Journal: Harris 2024 2-generation family, 1 affected, unaffected non-carrier parents M - United Kingdom (Great Britain) - - - - - ? see paper; .., macrocephaly, 3y6m-OFC 2.6, 9y9m-OFC +3.02; no ventriculomegaly; polydactyly; autistic; global developmental delay, 12m-sit, 24m-walk, 5y-speaks single words, 5y11m- 3-word sentences; delayed visual maturation; no cardiac phenotype; 4y-perianal abscesses 1 1 Johan den Dunnen
00445146 Pat3 PubMed: Harris 2024, Journal: Harris 2024 2-generation family, 1 affected, unaffected non-carrier parents M - Netherlands - - - - - ? see paper; .., OFC normal; no ventriculomegaly; polydactyly; atrial septal defect; hypospadias, renal agenesis, single umbilical artery, flattened thoracic vertebrae 1 1 Johan den Dunnen
00465239 patient - - M no (Brazil) - - - - - ? - 1 1 Juliana Mazzeu
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