Phenotypes for disease #04179 (AOS (Adams-Oliver syndrome (AOS)))

61 entries on 1 page. Showing entries 1 - 61.
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0000025737 scalp defect; TTLD of hands and feet; microcephaly; developmental delay; - - Familial, autosomal recessive 03y06m - - - - Maja Sukalo 00029773
0000025738 scalp defect; TTLD of hands and feet; aortic valve dysplasia; ventricular dilatation / brain atrophy; periventricular lesions (calcification, gliosis); abdominal skin defect; - - Familial, autosomal recessive 01y00m - - - - Maja Sukalo 00029774
0000025739 scalp defects; TTLD of hands and feet; ventricular dilatation / brain atrophy; periventricular lesions (calcification, gliosis); seizures / epilepsy; gastroschisis; - - Familial, autosomal recessive ? - - - - Maja Sukalo 00029775
0000025740 scalp defect; TTLD of hands and feet; periventricular lesions (calcification, gliosis); pachygyria; optic atrophy; seizures / epilepsy; - - Familial, autosomal recessive 02y00m - - - - Maja Sukalo 00029776
0000025741 IUGR; scalp defect; TTLD of hands and feet; tetralogy of Fallot; persistent left superior vena cava; periventricular lesions (calcification, gliosis); porencephaly; microcephaly; retinal detachment; severe ID; seizures / epilepsy; placental vasculopathy; neonatal thrombocytopenia; small bowel infarction; - - Familial, autosomal recessive 02y00m - - - - Maja Sukalo 00029777
0000025742 scalp defect; TTLD of hands and feet; microcephaly; microphthalmia; retinal detachment; vitreous opacities/membranes; anterior chamber abnormality; developmental delay; seizures / epilepsy; high palate; - - Familial, autosomal recessive 05y00m - - - - Maja Sukalo 00029778
0000025743 scalp defect; TTLD of hands and feet; ventricular dilatation / brain atrophy; corpus callosum hypoplasia/atrophy; microcephaly; ocular anomaly; severe ID; seizures / epilepsy; cerebral palsy / spasticity; CMTC; single umbilical artery; cryptorchidism; - - Familial, autosomal recessive 10y00m - - - - Maja Sukalo 00029779
0000025744 IUGR; scalp defect; TTLD of hands and feet; ventricular dilatation / brain atrophy; periventricular lesions (calcification, gliosis); microcephaly; microphthalmia; retinal detachment; anterior chamber abnormality; severe ID; seizures / epilepsy; cerebral palsy / spasticity; CMTC; abdominal skin defect; - - Familial, autosomal dominant 20y00m - - - - Maja Sukalo 00029780
0000025745 scalp defect; TTLD of hands and feet; patent ductus arteriosus; ventricular dilatation / brain atrophy; microcephaly; microphthalmia; knee dislocation; - - Familial, autosomal recessive 00y03m - - - - Maja Sukalo 00029781
0000025746 IUGR; scalp defect; TTLD of hands and feet; ventricular dilatation / brain atrophy; corpus callosum hypoplasia/atrophy; periventricular lesions (calcification, gliosis); microcephaly; microphthalmia; retinal detachment; moderate ID; seizures / epilepsy; cryptorchidism; - - Familial, autosomal recessive 09y00m - - - - Maja Sukalo 00029782
0000025747 scalp defect; TTLD of hands and feet; ventricular septal defect; ventricular dilatation / brain atrophy; periventricular lesions (calcification, gliosis); microcephaly; microphthalmia; retinal detachment; vitreous opacities/membranes; severe ID; seizures / epilepsy; cerebral palsy / spasticity; abdominal skin defects; absence of right patella; - - Familial, autosomal recessive ? - - - - Maja Sukalo 00029783
0000025748 IUGR; scalp defects; TTLD of hands and feet; ventricular dilatation / brain atrophy; corpus callosum hypoplasia/atrophy; retinal detachment; abdominal skin defect; patella fixed to skin; - - Familial, autosomal recessive 00y00m - - - - Maja Sukalo 00029784
0000025749 scalp defect; TTLD of hands and feet; brain anomalies; microcephaly; ocular anomalies; severe ID; seizures / epilepsy; abdominal skin defect; - - Familial, autosomal recessive 07y00m - - - - Maja Sukalo 00029785
0000025750 IUGR; TTLD of feet; total anomalous pulmonary venous connection; ocular anomalies; mild ID; hypothyroidism; - - Familial, autosomal recessive 08y00m - - - - Maja Sukalo 00029786
0000025751 scalp defect; TTLD of hands and feet; no further data available; - - Familial, autosomal recessive ? - - - - Maja Sukalo 00029787
0000025752 scalp defect; TTLD of hands and feet; periventricular lesions (calcification, gliosis); no further data available; - - Familial, autosomal recessive 07y00m - - - - Maja Sukalo 00029788
0000025753 scalp defect; TTLD of hands and feet; ventricular dilatation / brain atrophy; corpus callosum hypoplasia/atrophy; periventricular lesions (calcification, gliosis); microcephaly; seizures / epilepsy; - - Familial, autosomal recessive ? - - - - Maja Sukalo 00029789
0000025754 scalp defect; TTLD of hands and feet; ventricular dilatation / brain atrophy; periventricular lesions (calcification, gliosis); microcephaly; optic atrophy; severe ID; seizures / epilepsy; cerebral palsy / spasticity - - Familial, autosomal recessive 00y11m - - - - Maja Sukalo 00029772
0000025756 see paper; .. - - Familial, autosomal recessive - - - - - Johan den Dunnen 00029791
0000025757 - - - Familial, autosomal recessive - - - - - Johan den Dunnen 00029792
0000025774 see paper; syndactyly 2nd/3rd toes, otherwise normal, short palpebral fissures, mildly delayed gross motor milestones, microcephaly, aplasia cutis congenita scalp (HP:0007385) - - Familial, autosomal recessive 00y00m00d - - - - Johan den Dunnen 00029801
0000025775 see paper; shortened distal phalanges left hand, bilateral reduction toes, no intellectual disability - - Familial, autosomal dominant - - - - - Johan den Dunnen 00029802
0000025776 see paper; aplasia cutis congenita, bony defect/abnormal fontanelle, terminal transverse limb defects, syndactyly - - Familial, autosomal dominant - - - - - Johan den Dunnen 00029803
0000025777 see paper; aplasia cutis congenita, bony defect/abnormal fontanelle, terminal transverse limb defects, syndactyly - - Familial, autosomal dominant - - - - - Johan den Dunnen 00029804
0000025874 see paper; .. - - Familial, autosomal recessive - - - - - Johan den Dunnen 00032397
0000027454 - - - Familial - - - - - Maja Sukalo 00034059
0000027457 - - - Familial - - - - - Maja Sukalo 00034062
0000027458 - - - Familial - - - - - Maja Sukalo 00034063
0000027459 - - - Familial - - - - - Maja Sukalo 00034064
0000027460 - - - Familial - - - - - Maja Sukalo 00034065
0000027461 - - - Familial - - - - - Maja Sukalo 00034066
0000027462 - - - Familial - - - - - Maja Sukalo 00034067
0000027463 - - - Familial - - - - - Maja Sukalo 00034068
0000027464 - - - Familial - - - - - Maja Sukalo 00034069
0000027465 - - - Familial - - - - - Maja Sukalo 00034070
0000027466 - - - Familial - - - - - Maja Sukalo 00034071
0000027467 - - - Familial - - - - - Maja Sukalo 00034072
0000027468 - - - Familial - - - - - Maja Sukalo 00034073
0000027469 - - - Familial - - - - - Maja Sukalo 00034074
0000036656 no further details, aplasia cutis congenita scalp (HP:0007385) - - Isolated (sporadic) - - - - - Johan den Dunnen 00049883
0000036657 short distal phalangus middle finger right hand, symphalangism index finger, symbrachydactyly both feet; truncus arteriosus, ventricular septum defect; growth hormone deficiency, aplasia cutis congenita scalp (HP:0007385) - - Isolated (sporadic) - - - - - Johan den Dunnen 00049882
0000036668 no further details, aplasia cutis congenita scalp (HP:0007385) - - Isolated (sporadic) - - - - - Johan den Dunnen 00049877
0000036670 left brachydactyly 3rd4th toes (confirmed by X-ray), normal scalp - - Unknown - - - - - Johan den Dunnen 00049874
0000036671 short distal phalanges (not confirmed by X-ray), normal scalp - - Familial, autosomal dominant - - - - - Johan den Dunnen 00049893
0000036672 normal echocardiogram, aplasia cutis congenita scalp (HP:0007385) - - Familial, autosomal dominant - - - - - Johan den Dunnen 00049894
0000036673 brachydactyly, syndactyly 2nd/3rd toes right foot; tricuspid insufficiency, ventricular septum defect, aplasia cutis congenita scalp (HP:0007385) - - Familial, autosomal dominant - - - - - Johan den Dunnen 00049895
0000036674 ACC with underlying skull defect; brachydactyly left foot, missing toes right foot; normal echocardiogram, aplasia cutis congenita scalp (HP:0007385) - - Familial - - - - - Johan den Dunnen 00049896
0000036675 ACC with underlying skull defect; brachysyndactyly right foot, severe brachysyndactyly left foot; normal echocardiogram; small kidneys, mild hypertension, aplasia cutis congenita scalp (HP:0007385) - - Familial - - - - - Johan den Dunnen 00049897
0000036676 , aplasia cutis congenita scalp (HP:0007385) - - Familial - - - - - Johan den Dunnen 00049876
0000036677 , aplasia cutis congenita scalp (HP:0007385) - - Familial - - - - - Johan den Dunnen 00049898
0000036678 syndactyly 2nd/3rd toes, hypoplastic toe nails, brachydactyly toes - - Familial, autosomal dominant - - - - - Johan den Dunnen 00049878
0000036679 bald area on scal, cutis marmorata - - Familial, autosomal dominant - - - - - Johan den Dunnen 00049900
0000036680 bald area on scalp; brachydactyly fingers/toes, syndactyly 2nd/3rd toes - - Familial, autosomal dominant - - - - - Johan den Dunnen 00049901
0000036681 bald area on scalp - - Familial, autosomal dominant - - - - - Johan den Dunnen 00049903
0000036682 ACC with underlying skull defect, aplasia cutis congenita scalp (HP:0007385) - - Familial, autosomal dominant - - - - - Johan den Dunnen 00049904
0000036683 normal echocardiogram; cutis marmorata, epilepsy, learning difficulties, borderline intellectual function (TIQ 76) at young age, normal IQ at later age; mild periventricular leukomalacia, aplasia cutis congenita scalp (HP:0007385) - - Familial, autosomal dominant - - - - - Johan den Dunnen 00049905
0000036684 normal echocardiogram, portal hypertension; esophageal varices splenomegaly, congenital liver fibrosis, aplasia cutis congenita scalp (HP:0007385) - - Familial, autosomal dominant - - - - - Johan den Dunnen 00049906
0000036685 no cardiac problems, no dilatation, aplasia cutis congenita scalp (HP:0007385) - - Familial - - - - - Johan den Dunnen 00049879
0000036686 normal echocardiogram, aplasia cutis congenita scalp (HP:0007385) - - Familial - - - - - Johan den Dunnen 00049907
0000036687 delayed ossification; hypoplastic toe nails; no cardiac problems; cutis marmorata; 2m-normal chest X-ray, aplasia cutis congenita scalp (HP:0007385) - - Isolated (sporadic) - - - - - Johan den Dunnen 00049908
0000244360 stroke, abnormal cerebral morphology, leukoencephalopathy, vasculitis, abnormality of lysosomal metabolism, inflammatory arteriopathy, recurrent subcortical infarcts, abnormal cerebral artery morphology, abnormality of the cerebral subcortex, abnormal cellular physiology, abnormality of the cerebral vasculature - - Unknown 48y - - - - Andreas Laner 00325873
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