All individuals with variants in gene HDAC3

19 entries on 1 page. Showing entries 1 - 19.
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00050575 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected F - United Kingdom (Great Britain) - - - Decipher - ? intellectual disability, seizures 1 1 Johan den Dunnen
00303072 Pat114 PubMed: Helbig 2016 - - - United States - - - - - seizures Neonatal Epileptic Encephalopathy; age onset neonatal 1 1 Johan den Dunnen
00452992 Pat1 PubMed: Yoon 2024, Journal: Yoon 2024 2-generation family, 1 affected, unaffected non-carrier parents F - Korea, South (Republic) Asia - - - - NDD birth full-term, cesarean delivery, weight 1.98 kg; severe intellectual disability (HP:0001249); neurodevelopmental delay (HP:0012758); scoliosis, varus proximal tibia, hand joint deformity, musculoskeletal abnormalities (HP:0033127); seizure (HP:0001250); facial dysmorphism (HP:0001999); MRI brain normal (-HP:0410263); no abnormality genitourinary system (-HP:0000119); microcephaly (HP:0000252); sensorineural hearing impairment (HP:0000365); failure to thrive (HP:0001508); congenital heart disease (HP:0001627); autistic behavior (HP:0000729); microtia 1 1 Johan den Dunnen
00452993 Pat2 PubMed: Yoon 2024, Journal: Yoon 2024 2-generation family, 1 affected, unaffected non-carrier parents F - Korea, South (Republic) Asia - - - - NDD birth 36w, vaginal delivery, weight 2.10 kg; severe intellectual disability (HP:0001249); neurodevelopmental delay (HP:0012758); polydactyly, syndactyly, musculoskeletal abnormalities (HP:0033127); no seizure (-HP:0001250); facial dysmorphism (HP:0001999); MRI brain normal (-HP:0410263); congenital hydronephrosis (HP:0000119); microcephaly (HP:0000252); no hearing impairment (-HP:0000365); failure to thrive (HP:0001508); congenital heart disease (HP:0001627); no autistic behavior (-HP:0000729) 1 1 Johan den Dunnen
00452994 Pat3 PubMed: Yoon 2024, Journal: Yoon 2024 2-generation family, 1 affected, unaffected non-carrier parents M - United Kingdom (Great Britain) Europe - - - - NDD birth 40w, vaginal delivery, weight 3.30 kg; moderate intellectual disability (HP:0001249); neurodevelopmental delay (HP:0012758); no musculoskeletal abnormalities (-HP:0033127); seizure (HP:0001250); no facial dysmorphism -(HP:0001999); MRI brain subcortical heterotopia (HP:0410263); phimosis (HP:0000119); no microcephaly (-HP:0000252); no hearing impairment (-HP:0000365); no failure to thrive (-HP:0001508); no congenital heart disease (-HP:0001627); autistic behavior (HP:0000729) 1 1 Johan den Dunnen
00452995 Pat4 PubMed: Yoon 2024, Journal: Yoon 2024 2-generation family, 1 affected, unaffected non-carrier parents F - United Kingdom (Great Britain) Europe - - - - NDD mild intellectual disability (HP:0001249); neurodevelopmental delay (HP:0012758); ; joint hypermobility, musculoskeletal abnormalities (HP:0033127); no seizure (-HP:0001250); no facial dysmorphism -(HP:0001999); MRI brain focus of nodular heterotopia (HP:0410263); no abnormality genitourinary system (-HP:0000119); no microcephaly (-HP:0000252); no hearing impairment (-HP:0000365); no failure to thrive (-HP:0001508); no congenital heart disease (-HP:0001627); no autistic behavior (-HP:0000729); subcutaneous scalp arteriovenous malformation 1 1 Johan den Dunnen
00452996 Pat5 PubMed: Yoon 2024, Journal: Yoon 2024 2-generation family, 1 affected, unaffected non-carrier parents M - United Kingdom (Great Britain) Europe - - - - NDD birth 35w, vaginal delivery (dizygotic twin), weight 2.04 kg; moderate intellectual disability (HP:0001249); neurodevelopmental delay (HP:0012758); hand joint deformity, musculoskeletal abnormalities (HP:0033127); no seizure (-HP:0001250); facial dysmorphism (HP:0001999); MRI brain mildly dilated vestibular ducts (HP:0410263); congenital unilateral right hydronephrosis with vesicoureteral reflux (HP:0000119); no microcephaly (-HP:0000252); mixed type hearing impairment (HP:0000365); no failure to thrive (-HP:0001508); no congenital heart disease (-HP:0001627); no autistic behavior (-HP:0000729); type 1 diabetes, chronic acral warts 1 1 Johan den Dunnen
00452997 Pat6 PubMed: Yoon 2024, Journal: Yoon 2024 2-generation family, 1 affected, unaffected non-carrier parents M - United States Europe - - - - NDD birth full-term, vaginal delivery, weight 4.17 kg; no intellectual disability (-HP:0001249); no neurodevelopmental delay (-HP:0012758); neonatal torticollis, musculoskeletal abnormalities (HP:0033127); seizure (HP:0001250); no facial dysmorphism -(HP:0001999); MRI brain normal (-HP:0410263); no abnormality genitourinary system (-HP:0000119); no microcephaly (-HP:0000252); no hearing impairment (-HP:0000365); no failure to thrive (-HP:0001508); no congenital heart disease (-HP:0001627); no autistic behavior (-HP:0000729) 1 1 Johan den Dunnen
00453000 DECIPHER-4681 PubMed: Yoon 2024, Journal: Yoon 2024 2-generation family, 1 affected, unaffected non carrier parents F - - Europe - - - - NDD delayed speech and language development; feeding difficulties in infancy; hypotonia; intellectual disability; seizure 1 1 Johan den Dunnen
00453001 DECIPHER-307291 PubMed: Yoon 2024, Journal: Yoon 2024 2-generation family, 1 affected, unaffected non carrier parents F - - Europe - - - - NDD camptodactyly of finger; eczema; flexion contracture of toe; hypohidrosis 1 1 Johan den Dunnen
00453002 DECIPHER-253734 PubMed: Yoon 2024, Journal: Yoon 2024 2-generation family, 1 affected, unaffected non carrier parents M - - Europe - - - - NDD feeding difficulties in infancy; hypotonia; intellectual disability 1 1 Johan den Dunnen
00453003 DECIPHER-264075 PubMed: Yoon 2024, Journal: Yoon 2024 2-generation family, 1 affected, unaffected non carrier parents F - - Europe - - - - NDD abnormal plantar dermatoglyphics; broad face; lissencephaly; seizure 1 1 Johan den Dunnen
00453004 DECIPHER-249028 PubMed: Yoon 2024, Journal: Yoon 2024 2-generation family, 1 affected, unaffected non carrier parents F - - Europe - - - - NDD abnormality of the upper respiratory tract; coarse facial features; hypotonia; intellectual disability; patent ductus arteriosus 1 1 Johan den Dunnen
00453005 DECIPHER-293879 PubMed: Yoon 2024, Journal: Yoon 2024 - F - - Europe - - - - NDD - 1 1 Johan den Dunnen
00453006 DECIPHER-401315 PubMed: Yoon 2024, Journal: Yoon 2024 2-generation family, 1 affected, unaffected non carrier parents F - - Europe - - - - NDD abnormal pinna morphology; brachycephaly; constipation; deeply set eye; delayed speech and language development; diabetes mellitus; eeg abnormality; fine hair; gait disturbance; hypertelorism; intellectual disability; mandibular prognathia; precocious puberty in females; prominent nose; recurrent infections; scoliosis; short philtrum; strabismus; wide mouth 1 1 Johan den Dunnen
00453007 DECIPHER-345239 PubMed: Yoon 2024, Journal: Yoon 2024 - - - - Europe - - - - NDD - 1 1 Johan den Dunnen
00453008 DECIPHER-473002 PubMed: Yoon 2024, Journal: Yoon 2024 - F - - Europe - - - - NDD - 1 1 Johan den Dunnen
00453009 DECIPHER-255372 PubMed: Yoon 2024, Journal: Yoon 2024 2-generation family, 1 affected, unaffected non carrier parents F - - Europe - - - - NDD 2-3 toe syndactyly; inguinal hernia; intellectual disability; microcephaly; sacral dimple; seizure; short stature 1 1 Johan den Dunnen
00453010 DECIPHER-261240 PubMed: Yoon 2024, Journal: Yoon 2024 2-generation family, 1 affected, unaffected non carrier parents F - - Europe - - - - NDD intellectual disability; seizure 1 1 Johan den Dunnen
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