| Descriptor English: | Polycystic Kidney, Autosomal Recessive | ||||||
| Descriptor Spanish: |
Riñón Poliquístico Autosómico Recesivo
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| Descriptor Portuguese: | Rim Policístico Autossômico Recessivo | ||||||
| Descriptor French: | Polykystose rénale autosomique récessive | ||||||
| Entry term(s): |
ARPKD Autosomal Recessive Polycystic Kidney Autosomal Recessive Polycystic Kidney Disease Kidney, Polycystic, Autosomal Recessive Polycystic Kidney Disease, Autosomal Recessive Polycystic Kidney Disease, Infantile, Type 1 Polycystic Kidney Disease, Infantile, Type I Polycystic Kidney and Hepatic Disease 1 Polycystic Kidney and Hepatic Disease 1 (Autosomal Recessive) |
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| Tree number(s): |
C12.050.351.968.419.403.875.510 C12.200.777.419.403.875.510 C12.950.419.403.875.510 C16.131.077.717.510 C16.320.184.625.510 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D017044 | ||||||
| Scope note: | A genetic disorder with autosomal recessive inheritance, characterized by multiple CYSTS in both KIDNEYS and associated LIVER lesions. Serious manifestations are usually present at BIRTH with high PERINATAL MORTALITY. |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Previous Indexing: |
Kidney, Polycystic (1966-1991) |
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| Public MeSH Note: | 1992; see KIDNEY, POLYCYCSTIC, AUTOSOMAL RECESSIVE 1992-2000 |
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| History Note: | 1992 |
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| DeCS ID: | 30023 | ||||||
| Unique ID: | D017044 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1992/01/01 | ||||||
| Date of Entry: | 1991/05/30 | ||||||
| Revision Date: | 2017/12/14 |
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Polycystic Kidney, Autosomal Recessive
- Preferred
| Concept UI |
M0025899 |
| Scope note | A genetic disorder with autosomal recessive inheritance, characterized by multiple CYSTS in both KIDNEYS and associated LIVER lesions. Serious manifestations are usually present at BIRTH with high PERINATAL MORTALITY. |
| Preferred term | Polycystic Kidney, Autosomal Recessive |
| Entry term(s) |
ARPKD Autosomal Recessive Polycystic Kidney Autosomal Recessive Polycystic Kidney Disease Kidney, Polycystic, Autosomal Recessive Polycystic Kidney Disease, Autosomal Recessive Polycystic Kidney Disease, Infantile, Type 1 Polycystic Kidney Disease, Infantile, Type I Polycystic Kidney and Hepatic Disease 1 Polycystic Kidney and Hepatic Disease 1 (Autosomal Recessive) |
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