Latest Research
- Familial Hyperlipoproteinemia Type 1
- N-acetyl-alpha-D-galactosaminidase
- Multiple Endocrine Neoplasia- Type 2B
- Mobius Syndrome
- Cat Eye Syndrome
- Ankylostomiasis
- Winkelman Bethge Pfeiffer Syndrome
- Hyposmia Nasal Hypoplasia Hypogonadism
- Fetal Alcohol Syndrome
- Tuberculous Uveitis
- Hereditary Macrothrombocytopenia
- X-linked Ichthyosis
D in Research
- D-glycericacidemia
- D-minus hemolytic uremic syndrome (D-HUS)
- D-plus hemolytic uremic syndrome (D+HUS)
- Dandy Walker variant
- Dandy-Walker malformation with mental retardation- basal ganglia disease- and seizures
- Dandy-walker malformation with mental retardation- macrocephaly- myopia- and brachytelephalangy
- Daneman Davy Mancer syndrome
- Danubian endemic familial nephropathy
- Davenport Donlan syndrome
- Davis Lafer syndrome
- De Barsy syndrome
- De Hauwere Leroy Adriaenssens syndrome
- De Sanctis-Cacchione syndrome
- Deafness conductive ptosis skeletal anomalies
- Deafness conductive stapedial ear malformation facial palsy
- Deafness craniofacial syndrome
- Deafness enamel hypoplasia nail defects
- Deafness epiphyseal dysplasia short stature
- Deafness goiter stippled epiphyses
- Deafness hyperuricemia neurologic ataxia