Phenotypes for disease #00372 (CED (dysplasia, cranioectodermal (CED, Sensenbrenner syndrome)))

8 entries on 1 page. Showing entries 1 - 8.
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Individual ID     
0000015150 - - - Unknown - - - - - Heleen Arts 00016535
0000015165 - - - Unknown - - - - - Heleen Arts 00016536
0000073490 Cranioectodermal dysplasia-1 (CED1) - - Familial, autosomal recessive - - - - - Karen Stals 00095096
0000087174 Craniosynostosis sagittal (HPO:000442), Craniosynostosis coronal (HPO:000440), Dolichocephaly (HPO: ), Nephronophthisis (HPO:000090), Sate 2 chronic kidney disease (HPO:0012624), short limbs (HPO:0009826), Narrow thorax (HPO:0000774), Brachydactyly (HPO:0001156), Abnormal teeth (HPO:0000164), Everted lower lip (HPO:0000233), Epicanthic folds (HPO:0000286) - - Familial, autosomal recessive 01y 01y06m - - - Joanna Walczak-Sztulpa 00108617
0000223439 - - - Familial, autosomal recessive 01y 01y - - IFT121 Joanna Walczak-Sztulpa 00295963
0000227559 no dolichocephaly/scaphocephaly; no craniosynostosis; no frontal bossing; no macrocephaly; no telecanthus; no everted lower lip; no micrognathia; hypoplastic teeth; widely spaced teeth; short broad nails; fine hair; no skin laxity; dry skin; narrow thorax; no pectus excavatum; short humeri; brachydactyly; webbing of fingers; no postaxial polydactyly; restricted flexion of fingers; syndactyly of 2-3-4 toes; no bilateral sandal gap; joint laxity; nephronophthisis; no liver disease; no heart disease; no neurological findings; no recurrent lung infections, normal intelligence; height 112 cm (-2.5 SD) Sensenbrenner syndrome CED3 Familial, autosomal recessive 07y - - - - Johan den Dunnen 00300258
0000227560 scaphocephaly; sagittal suture synostosis; frontal bossing; no macrocephaly; telecanthus; everted lower lip; micrognathia; hypoplastic teeth; widely spaced teeth; short broad nails; sparse hair, fine hair; skin laxity; dry skin; narrow thorax; no pectus excavatum; bowing of humeri; brachydactyly; webbing of fingers; bilateral postaxial polydactyly feet, bilateral postaxial polydactyly hands; no restricted flexion of fingers; syndactyly of 2-3 and 5-6 toes; bilateral sandal gap; joint laxity; nephronophthisis, 3y-end-stage renal disease; neonatal cholestasis, liver cirrhosi; peripheral pulmonary stenosis; no neurological findings; no recurrent lung infections; normal intelligence; height 91 cm (<<-2.5 SD) Sensenbrenner syndrome CED3 Familial, autosomal recessive 05y - - - - Johan den Dunnen 00300259
0000350792 see paper Sensenbrenner syndrome - Unknown - - - - - Johan den Dunnen 00359412
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