All individuals with variants in gene DPF2

10 entries on 1 page. Showing entries 1 - 10.
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VIP     

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Variants     

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00125791 - Journal: Vasileiou 2018 - M no - - - - - - CSS photophobia; generalized hypotonia; 6m-feeding problems 1-2y; no seizures (-HP:0001250); delayed growth (HP:00001510); hearing loss (HP:0000365); speech delayed (HP:0000750); mild-moderate intellectual disability; abnormal behaviour (HP:0000708); sparse scalp hair (HP:0002209); thick eyebrow (HP:0000574); long eyelashes (HP:0000527); walk-17m; no ptosis (-HP:0000520); thick alae (HP:0009928); short philtrum (HP:0000322); wide mouth (HP:0000154); abnormality lower lip (HP:0000178); no cleft palate (-HP:0000175); ear abnormality (HP:0000598); no hypertrichosis (-HP:0000998); no scoliosis (-HP:0002650); no pectus excavatum (-HP:0000767); short 5th finger (HP:0009237); no absent 5th distal phalanx; multiple small nails; no delayed bone age (-HP:0003799);; no hypoplastic phalanges fingers/toes; joint laxity (HP:0001388); no intestinal anomalies (-HP:0002242), no gastro-esophoegal reflux (-HP:0002020); no cardiac abnormality (-HP:0001627); no kidney abnormality (-HP:0000077); small teeth (HP:0000691); recurrent infections (HP:0002719); MRI brain normal; no pyloric stenosis (-HP:0002021); no inguinal hernia (-HP:0000023); hypermetropia (HP:000540), no coloboma (-HP:0000589); normal eye movement (-HP:0000496) 1 1 Bernt Popp
00131901 - Journal: Vasileiou 2018 - F no - - - - - - CSS - 1 1 Georgia Vasileiou
00131902 - Journal: Vasileiou 2018 - F yes - - - - - - CSS - 1 1 Georgia Vasileiou
00131903 - Journal: Vasileiou 2018 - M no - - - - - - CSS - 1 1 Georgia Vasileiou
00131904 - Journal: Vasileiou 2018 - M no - - - - - - CSS - 1 1 Georgia Vasileiou
00131905 - Journal: Vasileiou 2018 - F no - - - - - - CSS - 1 1 Georgia Vasileiou
00131906 - Journal: Vasileiou 2018 - F no - - - - - - CSS - 1 1 Georgia Vasileiou
00131907 - Journal: Vasileiou 2018 - M no - - - - - - CSS - 1 1 Georgia Vasileiou
00228896 - - - F no New Zealand - - - - - CSS - 1 1 Louise Bicknell
00467742 Pat14 PubMed: Bou-Rouphael 2025, Journal: Bou-Rouphael 2025 2-generation family, 1 affected, unaffected non-carrier mother M - - - - - - - NDD see paper; ..., moderate intellectual developmental disorder; 12m-walk; 9y-first words; speech sentences; autism spectrum disorder; attention-deficit/hyperactivity disorder, prior violent behavior; no seizures; narrow ears, mild synorphrys; normal extremities; no postnatal growth retardation; obesity during chilhood 1 1 Johan den Dunnen
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