Phenotypes for disease #03242 (MACS (MACS syndrome (MACS, macrocephaly, alopecia, cutis laxa, and scoliosis)), OMIM:613075)

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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     
0000203692 height 111cm (-0.6 SD), no polydactyly, no walking difficulties, no speech impairment, no blindness, macrocephaly, no alopecia, no scoliosis, no cutis laxa, umbilical hernia, facial coarsening RIN2 syndrome MACS Familial, autosomal recessive 06y - - - - Sadaf Naz 00265914
0000203693 height 96cm (-1.3 SD), no polydactyly, no walking difficulties, no speech impairment, no blindness, macrocephaly, alopecia, scoliosis, no cutis laxa, umbilical hernia, facial coarsening RIN2 syndrome MACS Familial, autosomal recessive 04y - - - - Sadaf Naz 00265915
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