Phenotypes for disease #00612 (CSA (Cockayne syndrome, type A (CSA)), OMIM:216400)

3 entries on 1 page. Showing entries 1 - 3.
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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     
0000044551 Microcephaly HP:0000252 - - Familial, autosomal recessive - - - - - Birgit Sikkema-Raddatz 00057256
0000268944 HP:0001276; HP:0001249; HP:0006817; HP:0000238; HP:0100702; HP:0001263; HP:0000750; HP:0001181; HP:0002194; HP:0010862; HP:0001883 - Cockayne syndrome, type A (OMIM 216400) Familial, autosomal recessive - - - - - Wenjuan Qiu 00373719
0000308359 brain magnetic resonance imaging: leucodystrophy, cerebral and cerebellar atrophy; additional clinical featuresshort stature, truncal hypotonia, spasticity, contractures, scoliosis, deafness, pigmentary retinopathy, mildly enlarged liver and elevated aminotransferase, feeding problems, cryptorchid testis, severe developmental delay, progressive disease course (consanguineous parents) - Cockayne syndrome type A [MIM 216400] Familial, autosomal recessive 3y - - - - LOVD 00416849
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