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Renal agenesis, bilateral

Disease definition

A form of renal agenesis characterized by complete absence of kidney development, absent ureters and subsequent absence of fetal renal function resulting in Potter sequence with pulmonary hypoplasia related to oligohydramnios, which is fatal shortly after birth.

ORPHA:1848

Classification level: Subtype of disorder
  • Synonym(s): -
  • Prevalence: Unknown
  • Inheritance: Autosomal recessive 
  • Age of onset: Antenatal, Neonatal
  • ICD-10: Q60.1
  • ICD-11: LB30.00
  • OMIM: 191830  615721  617805  619887
  • UMLS: C1609433
  • MeSH: C536482
  • GARD: -
  • MedDRA: -

  A summary on this disease is available in Español (2014) Français (2014) Nederlands (2014) Suomi (2014, pdf)

Additional information

Further information on this disease

Patient-centred resources for this disease

Research activities on this disease

Specialised Social Services

Newborn screening

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.