Other disorders resulting from impaired renal tubular function

Preferred Label : Other disorders resulting from impaired renal tubular function;

Diag associé à un acte (%) : 60.0;

CMA : 2;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

N258;

UMLS CUI

C0477748;

Currated CISMeF NLP mapping
- secondary hyperparathyroidism of renal origin [SNOMED Notion]
Excluded by
- Secondary hyperparathyroidism, not elsewhere classified [ICD-10 Sub-category]
Orphanet concepts
- Autosomal dominant distal renal tubular acidosis [ORDO Disease]
- Autosomal dominant proximal renal tubular acidosis [ORDO Disease]
- Autosomal recessive distal renal tubular acidosis [ORDO Disease]
- Autosomal recessive distal renal tubular acidosis with deafness [ORDO Disease]
- Autosomal recessive distal renal tubular acidosis without deafness [ORDO Disease]
- Autosomal recessive proximal renal tubular acidosis [ORDO Disease]
- Dent disease [ORDO Disease]
- Dent disease type 1 [ORDO Disease]
- Dent disease type 2 [ORDO Disease]
- Distal renal tubular acidosis [ORDO Disease]
- Distal renal tubular acidosis with anemia [ORDO Disease]
- Dominant hypophosphatemia with nephrolithiasis or osteoporosis [ORDO Disease]
- Fanconi syndrome-ichthyosis-dysmorphism syndrome [ORDO Disease]
- Generalized pseudohypoaldosteronism type 1 [ORDO Disease]
- Hereditary renal hypouricemia [ORDO Disease]
- Hyperkalemic renal tubular acidosis [ORDO Disease]
- Hypohidrosis-electrolyte imbalance-lacrimal gland dysfunction-ichthyosis-xerostomia syndrome [ORDO Disease]
- Kidney tubulopathy-dilated cardiomyopathy syndrome [ORDO Disease]
- Primary renal tubular acidosis [ORDO Disease]
- Proximal renal tubular acidosis [ORDO Disease]
- Pseudohypoaldosteronism type 1 [ORDO Disease]
- Renal pseudohypoaldosteronism type 1 [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
Validated automatic mappings to BTNT
- Tubular disorders of sodium or potassium transport [ICD-11 Sub-sub category]

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