Phenotypes for disease #05193 (SEMDFA (dysplasia, spondylopeimetaphyseal, Faden-Alkuraya type (SEMDFA)), OMIM:616723)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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Owner     

Individual ID     
0000073557 diagnosed as Progressive Skeletal Dysplasia; short stature (HP:0004322), Intellectual disability (HP:0001249), Motor delay (HP:0001270), Delayed skeletal maturation (HP:0002750), Microcephaly (HP:0000252), Abnormal facial shape (HP:0001999), Overlapping toe (HP:0001845), Scoliosis (HP:0002650), no craniosynostosis (-HP:0001363), Carpal bone hypoplasia (HP:0001498), Platyspondyly (HP:0000926), Short femoral neck (HP:0100864), Short fourth metatarsal (HP:0004689), Cupped metaphyses of hand bones (HP:0004273) - - Familial, autosomal recessive 07y06m - - - - Pieter Klap 00065293
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