Disease Index
9,486 diseasesRefractory cytopenia with multilineage dysplasia
disease
ICD: D46.7
Regional odontodysplasia
tooth disease
ICD: K00.4MeSH: D018126
regional variant of Guillain-Barre syndrome
human disease
regressive spondylometaphyseal dysplasia
human disease
Reinhardt-Pfeiffer mesomelic dysplasia
Mesomelic dwarfism, Reinhardt-Pfeiffer type is characterized by disproportionate short stature from birth with dysplasia of the ulna and fibula
MeSH: C537349
Reis-Bücklers corneal dystrophy
disease of the human eye
MeSH: C535476
relapsing epidemic typhus
human disease
relapsing fever borreliosis
primary bacterial infectious disease that results in infection, has material basis in Borrelia, which is transmitted by tick or transmitted by body louse
MeSH: D012061
relapsing polychondritis
human disease
MeSH: D011081
renal agenesis
congenital disorder of urinary system
ICD: Q60.2
renal agenesis, unilateral
Unilateral renal agenesis (URA) is a form of renal agenesis (see this term) characterized by the complete absence of development of one kidney accompanied by an absent ureter
renal caliceal diverticuli-deafness syndrome
human disease
renal cell carcinoma
renal carcinoma that has material basis in the lining of the proximal convoluted renal tubule of the kidney
ICD: C64MeSH: D002292
renal cell carcinoma associated with neuroblastoma
Renal cell carcinoma that develops in patients who are long-term survivors of childhood neuroblastoma
renal coloboma syndrome
autosomal dominant disease characterized by optic nerve coloboma and renal disease
MeSH: C537168
renal disease with cataract
human disease
Renal dysplasia
ICD: Q61.4
renal dysplasia-limb defects syndrome
medical condition
MeSH: C537754
renal dysplasia, bilateral
renal dysplasia, unilateral
renal glycosuria
Human disease
MeSH: D006030
renal hypomagnesemia 2
hypomagnesemia characterized by autosomal dominant inheritance of hypomagnesemia due to renal magnesium loss that has material basis in heterozygous mutation in the FXYD2 gene on chromosome 11q23
MeSH: C537152
renal hypomagnesemia 3
hypomagnesemia characterized by autosomal recessive inheritance of excessive urinary Ca(2+) and Mg(2+) excretion that has material basis in homozygous or compound heterozygous mutation in the CLDN16 gene on chromosome 3q28
MeSH: C537153
renal hypomagnesemia 4
hypomagnesemia characterized by isolated hypomagnesemia due to renal loss with normal serum calcium levels and urinary calcium excretion that has material basis in variation in the chromosome region 4q25
MeSH: C567127
renal hypomagnesemia 5 with ocular involvement
human disease
MeSH: C536148
renal hypomagnesemia 6
human disease
renal hypoplasia
kidney disease that is characterized by abnormally small kidneys with normal morphology and reduced number of nephrons
ICD: Q60.5
renal hypoplasia, bilateral
Bilateral renal hypoplasia is a form of renal hypoplasia (see this term), a renal developmental anomaly in which both kidneys are small and have a deficit in the number of nephrons present
renal hypoplasia, unilateral
Unilateral renal hypoplasia is a form of renal hypoplasia (see this term), a renal developmental anomaly in which one kidney is small and has a deficit in the number of nephrons present
Renal medullary carcinoma
medical condition