Phenotypes for disease #03459 (anemia, megaloblastic (anemia, megaloblastic, due to dihydrofolate reductase deficiency), OMIM:613839)

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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     
0000274951 (+) Urinary retention,(+) Eczema,(+) Spasticity,(+) Global developmental delay,(+) Flexion contracture,(+) Talipes equinovalgus,(+) Talipes,(+) Constipation,(+) Lower limb spasticity,(+) Cerebral calcification,(+) Scoliosis,(+) Thoracolumbar scoliosis,(+) Limb joint contracture,(+) Abnormal hip bone morphology,(+) Abdominal symptom,(+) Abnormality of folate metabolism,(+) Chronic constipation,(+) Abnormality of digestive system physiology,(+) Abdominal cramps,(+) Flatulence,(+) Contractures of the joints of the upper limbs - - Familial, autosomal recessive - - - - - Andreas Laner 00381100
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