Phenotypes for disease #02804 (SMDCRD (dysplasia, spondylometaphyseal, with cone-rod dystrophy (SMDCRD)), OMIM:608940)

14 entries on 1 page. Showing entries 1 - 14.
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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     
0000074174 pigmentary maculopathy (HP:0008002), 13y6m cone-rod dystrophy (HP:0000548), short stature (HP:0003502), bowing long bones (HP:0006487), platyspondyly (HP:0000926), metaphyseal irregularities (HP:0003025), metaphyseal cupping (HP:0003021), decreased visual acuity (HP:0007663) - best coorect 20/100 - - Familial, autosomal recessive - - 7m - - Johan den Dunnen 00095884
0000074175 pigmentary maculopathy (HP:0008002), 17m cone-rod dystrophy (HP:0000548), short stature (HP:0003502), bowing long bones (HP:0006487), platyspondyly (HP:0000926), metaphyseal irregularities (HP:0003025), metaphyseal cupping (HP:0003021), decreased visual acuity (HP:0007663) - best coorect 20/180 - - Familial, autosomal recessive - - 1y1m - - Johan den Dunnen 00095885
0000074176 pigmentary maculopathy (HP:0008002), 51y cone-rod dystrophy (HP:0000548), short stature (HP:0003502), bowing long bones (HP:0006487), platyspondyly (HP:0000926), metaphyseal irregularities (HP:0003025), metaphyseal cupping (HP:0003021), decreased visual acuity (HP:0007663) - best coorect 8/80 - - Familial, autosomal recessive - - 51y - - Johan den Dunnen 00095886
0000074177 pigmentary maculopathy (HP:0008002), 36m cone-rod dystrophy (HP:0000548), bowing long bones (HP:0006487), platyspondyly (HP:0000926), metaphyseal irregularities (HP:0003025), metaphyseal cupping (HP:0003021), decreased visual acuity (HP:0007663) - best coorect 5/250 - - Familial, autosomal recessive - - 36m - - Johan den Dunnen 00095887
0000074178 pigmentary maculopathy (HP:0008002), 27m cone-rod dystrophy (HP:0000548), short stature (HP:0003502), bowing long bones (HP:0006487), platyspondyly (HP:0000926), metaphyseal irregularities (HP:0003025), metaphyseal cupping (HP:0003021), decreased visual acuity (HP:0007663) - best coorect 20/250 - - Familial, autosomal recessive - - 27m - - Johan den Dunnen 00095888
0000074179 pigmentary maculopathy (HP:0008002), bowing long bones (HP:0006487), platyspondyly (HP:0000926), metaphyseal irregularities (HP:0003025), metaphyseal cupping (HP:0003021), decreased visual acuity (HP:0007663) - best coorect 10/250 - - Familial, autosomal recessive - - 2y - - Johan den Dunnen 00095889
0000074180 pigmentary maculopathy (HP:0008002), 11y cone-rod dystrophy (HP:0000548), short stature (HP:0003502), bowing long bones (HP:0006487), platyspondyly (HP:0000926), metaphyseal irregularities (HP:0003025), metaphyseal cupping (HP:0003021) - - Familial, autosomal recessive - - 6m - - Johan den Dunnen 00095890
0000074181 pigmentary maculopathy (HP:0008002), cone-rod dystrophy (HP:0000548), short stature (HP:0003502), bowing long bones (HP:0006487), platyspondyly (HP:0000926), metaphyseal irregularities (HP:0003025), metaphyseal cupping (HP:0003021) - - Familial, autosomal recessive - - 23m - - Johan den Dunnen 00095891
0000074182 see paper; …, onset infancy - - Familial, autosomal recessive - - - - - Johan den Dunnen 00095892
0000074183 see paper; …, onset infancy - - Familial, autosomal recessive - - - - - Johan den Dunnen 00095893
0000074184 see paper; … - - Familial, autosomal recessive - - 11y - - Johan den Dunnen 00095894
0000074185 see paper; … - - Familial, autosomal recessive - - 14y - - Johan den Dunnen 00095895
0000074188 developmental delay moderate (HP:0001263), intellectual disability (HP:0002342), autism (HP:0000717), hypotonia (HP:0001252), sit 9m, walk 3y, 5y-generalised tonic clonic seizures (now seizure free), hand flapping, self-injurious behaviours, aggressive behaviour, inappropriate laughter, wide-based gait, exercise intolerance, strabismus, gastro-oesophageal reflux disease, constipstion, MRI-brain normal, midface retrusion, thin vermillion upper lip - - Isolated (sporadic) 11y - - - - Johan den Dunnen 00095908
0000104274 - - - Familial, autosomal recessive - - - - - Karina Silveira 00132071
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