Symptoms

The first step in rare disease diagnosis is to assess the patient's health and phenotypic information. We have compiled some general information for combinations of phenotypes that appear in the clinic. For each set of symptoms we show related diseases and genetic information. Once a medical doctor has found a potential diagnosis, the causative mutation can be confirmed through genotyping or sequencing.

Signs and Symptoms by name

Name
Anemia and Constipation, related diseases and genetic alterations View info
Anemia and Cough, related diseases and genetic alterations View info
Anemia and Cryptorchidism, related diseases and genetic alterations View info
Anemia and Cyanosis, related diseases and genetic alterations View info
Anemia and Dandy-Walker malformation, related diseases and genetic alterations View info
Anemia and Dehydration, related diseases and genetic alterations View info
Anemia and Delayed puberty, related diseases and genetic alterations View info
Anemia and Dementia, related diseases and genetic alterations View info
Anemia and Depressivity, related diseases and genetic alterations View info
Anemia and Diarrhea, related diseases and genetic alterations View info
Anemia and Difficulty walking, related diseases and genetic alterations View info
Anemia and Dilated cardiomyopathy, related diseases and genetic alterations View info
Anemia and Distal muscle weakness, related diseases and genetic alterations View info
Anemia and Dolichocephaly, related diseases and genetic alterations View info
Anemia and Dry skin, related diseases and genetic alterations View info
Anemia and Dysarthria, related diseases and genetic alterations View info
Anemia and Dysmetria, related diseases and genetic alterations View info
Anemia and Dysphagia, related diseases and genetic alterations View info
Anemia and Dystonia, related diseases and genetic alterations View info
Anemia and Ectodermal dysplasia, related diseases and genetic alterations View info