Phenotypes for disease #03686 (ACRDYS2 (acrodysostosis, with/without hormone resistance, type 2), OMIM:614613)

31 entries on 1 page. Showing entries 1 - 31.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000050888 advanced bone age; nasal hypoplasia; depressed nasal bridge; prominent mandible; severe brachydactyly; short metatarsals, metacarpals, and phalanges; cone-shaped epiphyses; speech delay, psychomotoer delay (walked at 17m of age); intracranial hypertension with thrombophlebitis of the transverse sinus and jugular - - Familial, autosomal dominant 4y - - - - Johan den Dunnen 00064690
0000050889 intrauterine growth retardation; advanced bone age; nasal hypoplasia; depressed nasal bridge; severe brachydactyly; short metatarsals, metacarpals, and phalanges; cone-shaped epiphyses; speech delay requiring orthophony, fine-motor-skill impairment; intracranial hypertension with jugular stenosis requiring derivation - - Familial, autosomal dominant 7y - - - - Johan den Dunnen 00064691
0000050890 - - - Isolated (sporadic) - - - - - Danielle Lynch 00064692
0000050891 advanced bone age; nasal hypoplasia; depressed nasal bridge; severe brachydactyly; short metatarsals, metacarpals, and phalanges; cone-shaped epiphyses; speech delay requiring orthophony, fine-motor-skill impairment - - Familial, autosomal dominant 4y - - - - Johan den Dunnen 00064693
0000050892 small hands, midface hypoplasia - - Familial, autosomal dominant - - - - - Johan den Dunnen 00064694
0000050893 - - - Isolated (sporadic) - - - - - Danielle Lynch 00064695
0000050895 - - - Isolated (sporadic) - - - - - Danielle Lynch 00064697
0000050896 advanced bone age; nasal hypoplasia; depressed nasal bridge; severe brachydactyly; short metatarsals, metacarpals, and phalanges; cone-shaped epiphyses; speech delay, psychomotor delay requiring physiotherapy - - Familial, autosomal dominant 3y - - - - Johan den Dunnen 00064698
0000050897 mild short stature, small hands, midface hypoplasia, lumbar stenosis; significant developmental disability; cryptorchidism - - Familial, autosomal dominant - - - - - Johan den Dunnen 00064699
0000050898 mild short stature, small hands, midface hypoplasia, lumbar stenosis; mild developmental disability; congenital hypothyroidism - - Familial, autosomal dominant - - - - - Johan den Dunnen 00064700
0000060303 PTH resistance, TSH resistance, obesity, mental retardation, craniosynostosis - - Familial, autosomal dominant - 07y - - - Francesca Marta Elli 00080728
0000060305 TSH resistance, short stature, obesity, brachydactily, mental rtardation cholelithiasis - - Unknown - 47y - - - Francesca Marta Elli 00080729
0000060306 short stature, obesity, dysmorphic facies, brachydactily, mental retardation - - Familial, autosomal dominant - 04y - - - Francesca Marta Elli 00080730
0000060307 short stature, obesity, dysmorphic facies, brachydactily, mental retardation, cryptorchidism, vesicoureteral reflux - - - - 29y - - - Francesca Marta Elli 00080732
0000060317 PTH resistance, dysmorphic facies, btachydactily, shypo-deformity of knees - - Unknown - 03y - - - Francesca Marta Elli 00080740
0000060318 short stature, dysmorphic facies, brachydactily, mental retardation, shypo-deformity of knees and shoulders - - Unknown - 15y - - - Francesca Marta Elli 00080741
0000060338 dysmorphic facies, brachydactily, mental retardation, failure to thrive, shypo-deformity of knees and shoulders - - Unknown - 0,9y - - - Francesca Marta Elli 00080759
0000060339 transient PTH resistance, short stature, dysmorphic facies, brachydactily, mental retardation, recurrent otitis media, cryptorchidism - - Unknown - 3.5y - - - Francesca Marta Elli 00080760
0000060340 PTH resistance, short stature, obesity, dysmorphic facies, brachydactily, mental retardation, DMT1, recurrent otitis media, lack of puberal growth spurt - - - - 14.7y - - - Francesca Marta Elli 00080761
0000060341 PTH resistance, short stature, dysmorphic facies, brachydactily, mental retardation, recurrent otitis media, hypertension, aortic valve insufficiency - - - - 12.5y - - - Francesca Marta Elli 00080762
0000060342 PTH resistance, short stature, obesity, dysmorphic facies, btachydactily, mental retardation, recurrent otitis media - - - - 07y - - - Francesca Marta Elli 00080764
0000060343 short stature, obesity, dysmorphic facies, brachydactily, mental retardation, recurrent otitis media, unilateral hydronephrosis - - - - 3.5y - - - Francesca Marta Elli 00080765
0000060344 short stature, obesity, dysmorphic facies, brachydactily, mental retardation, cone-shaped epiphyses, advanced bone age - - - - 14y - - - Francesca Marta Elli 00080766
0000060345 obesity, dysmorphic facies, brachydatily, mental retardation, cone-shaped epiphyses, advanced bone age - - - - 07y - - - Francesca Marta Elli 00080767
0000060346 borderline PTH resistance, short stature, dysmorphic facies, brachydactily, mental retardation, advanced bone age - - Familial, autosomal dominant - 39y&37y - - - Francesca Marta Elli 00080769
0000060347 short stature, dysmorphic facies, brachydactily, mental retardation, advancd bone age - - - - 10.5y - - - Francesca Marta Elli 00080770
0000060348 dysmorphic facies, brachydactily, mental retardation, advanced bone age - - - - 8.5y - - - Francesca Marta Elli 00080771
0000060349 short stature, dysmorphic facies, brachydactily, mental retardation, advanced bone age - - - - 17y - - - Francesca Marta Elli 00080772
0000060350 short stature, dysmorphic facies, brachydactily, mental retardation, advanced bone age - - Familial, autosomal dominant - 17y&4.11y - - - Francesca Marta Elli 00080773
0000104163 severe brachydactyly; thick hair; hypertrichosis arms; hip bone replacement–osteoarthrosis; abnormal stature, normal teeth; mil/moderate intellectual disability; dysmorphic face; no clacifications; normal calcium homeastasis; high circulating parathyroid hormone (HP:0003165); vitamin D deficiency (HP:0100512) - - Unknown 35y 35y - - - Arrate Pereda 00131945
0000239605 neurodevelopmental abnormality, global developmental delay, short stature, facial abnormality; delayed growth; progressive intellectual disability (HP:0006887); dysmorphic face (HP:0001999); decreased body weight (HP:0004325) 1 - Unknown - - - - - Andreas Laner 00315859
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