Phenotypes for disease #04327 (CRS (craniosynostosis (CRS)))

46 entries on 1 page. Showing entries 1 - 46.
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0000036723 nicoronal synostosis also present in mother - - Familial, autosomal recessive - - - - - Johan den Dunnen 00050112
0000049861 Right coronal suture synostosis bilateral camptodactyly of the fifth fingers divergent strabismus recurrent airway infections mild learning problems - - Familial, autosomal dominant - 4.5m 00y00m00d birth - Jacqueline Goos 00063257
0000058844 - - - Unknown - - - - - Kerry Miller 00079117
0000058845 Flat mid-face, down-slanting palpebral fissures, low set ears, facial asymmetry, retracted pre-maxilla, right choanal stenosis, micrognathia, peg-like teeth with conical incisors, absent lateral incisors, pectus excavatum, scoliosis, long palms, slight digital shortening, mild 4/5 syndactyly of toes, Chiari malformation, moderate - severe learning difficulties. - - Isolated (sporadic) - - - - - Kerry Miller 00079118
0000058846 Learning difficulties - - Isolated (sporadic) - - - - - Kerry Miller 00079119
0000125628 bicoronal synostosis (HP:0011318), sagittal craniosynostosis (HP:0004442) craniosynostosis affecting bilateral coronal and sagittal sutures - Unknown - - - - - Anshuman Sewda 00152044
0000125629 bicoronal synostosis (HP:0011318) craniosynostosis affecting bilateral coronal sutures - Unknown - - - - - Anshuman Sewda 00152526
0000125630 unicoronal synostosis, left (HP:0011315) craniosynostosis affecting left coronal sutures - Unknown - - - - - Anshuman Sewda 00152529
0000125631 unicoronal synostosis, left (HP:0011315) craniosynostosis affecting left coronal sutures - Unknown - - - - - Anshuman Sewda 00152003
0000125632 unicoronal synostosis, right (HP:0011315) craniosynostosis affecting right coronal sutures - Unknown - - - - - Anshuman Sewda 00152528
0000125633 sagittal craniosynostosis (HP:0004442) sagittal craniosynostosis - Unknown - - - - - Anshuman Sewda 00152530
0000125634 sagittal craniosynostosis (HP:0004442) sagittal craniosynostosis - Unknown - - - - - Anshuman Sewda 00152527
0000125635 sagittal craniosynostosis (HP:0004442) sagittal craniosynostosis - Unknown - - - - - Anshuman Sewda 00152011
0000219686 see paper; ..., neonatal microcephaly, agenesis corpus callosum, brachycephaly with reduced volume posterior fossa, cerebellar and pons hypoplasia, scoliosis, tethered cord (closed neural tube defect) craniosynostosis BAIDCS Familial, autosomal dominant - - - - - Johan den Dunnen 00285854
0000219687 see paper; ..., neonatal microcephaly, agenesis corpus callosum, brachycephaly with reduced volume posterior fossa, cerebellar and pons hypoplasia, scoliosis, tethered cord (closed neural tube defect) craniosynostosis BAIDCS Familial, autosomal dominant - - - - - Johan den Dunnen 00285855
0000219729 mother cranial dysmorphism; two children sagittal craniosynostosis craniosynostosis - Familial, autosomal dominant - - - - - Johan den Dunnen 00285887
0000219730 sagittal craniosynostosis craniosynostosis - Isolated (sporadic) - - - - - Johan den Dunnen 00285888
0000219731 sporadic metopic craniosynostosis craniosynostosis - Isolated (sporadic) - - - - - Johan den Dunnen 00285889
0000219764 sagittal craniosynostosis, metopic craniosynostosis craniosynostosis - Di-genic - - - - - Johan den Dunnen 00285891
0000219765 sagittal craniosynostosis craniosynostosis - Di-genic - - - - - Johan den Dunnen 00285892
0000219766 sagittal craniosynostosis, metopic craniosynostosis craniosynostosis - Di-genic - - - - - Johan den Dunnen 00285893
0000219767 sagittal craniosynostosis craniosynostosis - Di-genic - - - - - Johan den Dunnen 00285894
0000219768 sagittal craniosynostosis craniosynostosis - Di-genic - - - - - Johan den Dunnen 00285895
0000219769 sagittal craniosynostosis craniosynostosis - Di-genic - - - - - Johan den Dunnen 00285896
0000219770 metopic craniosynostosis craniosynostosis - Di-genic - - - - - Johan den Dunnen 00285897
0000219771 metopic craniosynostosis craniosynostosis - Di-genic - - - - - Johan den Dunnen 00285898
0000219772 metopic craniosynostosis craniosynostosis - Di-genic - - - - - Johan den Dunnen 00285899
0000219773 metopic craniosynostosis craniosynostosis - Isolated (sporadic) - - - - - Johan den Dunnen 00285900
0000219774 metopic craniosynostosis craniosynostosis - Di-genic - - - - - Johan den Dunnen 00285901
0000219775 metopic craniosynostosis craniosynostosis - Di-genic - - - - - Johan den Dunnen 00285902
0000219776 metopic craniosynostosis craniosynostosis - Di-genic - - - - - Johan den Dunnen 00285903
0000219777 - - - Di-genic - - - - - Johan den Dunnen 00285904
0000219778 - - - Di-genic - - - - - Johan den Dunnen 00285905
0000219781 sagittal craniosynostosis craniosynostosis - Di-genic - - - - - Johan den Dunnen 00285908
0000219783 metopic craniosynostosis craniosynostosis - Di-genic - - - - - Johan den Dunnen 00285910
0000219794 see paper; ..., sagittal craniosynostosis, coronal craniosynostosis, recurrence of CS within two months initial surgery requiring second operatio craniosynostosis - Di-genic - - - - - Johan den Dunnen 00285921
0000219795 metopic craniosynostosis craniosynostosis - Di-genic - - - - - Johan den Dunnen 00285923
0000219796 metopic craniosynostosis craniosynostosis - Di-genic - - - - - Johan den Dunnen 00285927
0000219797 metopic craniosynostosis craniosynostosis - Di-genic - - - - - Johan den Dunnen 00285929
0000219798 metopic craniosynostosis craniosynostosis - Di-genic - - - - - Johan den Dunnen 00285932
0000268614 - - - Isolated (sporadic) - - - - - Stuart Scott 00373335
0000326766 see paper; ..., hypoplasia or abscent corpus callosum, ventriculomegaly, lambdoid craniosynostosis, macrocephaly, develomental delay, dysmorphic features, no urinary tract defects craniosynostosis BRMUTD Familial, autosomal dominant 13y - - - - Johan den Dunnen 00436630
0000326767 see paper; ..., hypoplasia or abscent corpus callosum, ventriculomegaly, no craniosynostosis, macrocephaly, develomental delay, dysmorphic features, urinary tract defects craniosynostosis BRMUTD Familial, autosomal dominant 10y - - - - Johan den Dunnen 00436631
0000326768 see paper; ..., hypoplasia or abscent corpus callosum, ventriculomegaly, lambdoid craniosynostosis, macrocephaly, develomental delay, dysmorphic features, no urinary tract defects craniosynostosis BRMUTD Familial, autosomal dominant 6y - - - - Johan den Dunnen 00436632
0000326769 see paper; ..., hypoplasia or abscent corpus callosum, no ventriculomegaly, sagittal craniosynostosis, macrocephaly, no develomental delay, no dysmorphic features, urinary tract defects craniosynostosis BRMUTD Familial, autosomal dominant 42y - - - - Johan den Dunnen 00436633
0000338888 true hypotelorism, severe microcephaly, residual retrognathia, high arched palate with bifid uvula, dental crowding, mild scoliosis and generalized joint hypermobility with Beighton score 6/9, cleft palate - microcephaly, developmental delay and skeletal anomalies (MISA syndrome) Familial, autosomal dominant - - - - - Carmela Fusco 00449718
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