Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the kidney (HP:0000077)help
Grandparent Node:
expandAbnormality of the urinary system physiology (HP:0011277)help
Parent Node:
expandAbnormal renal physiology (HP:0012211)help
..Starting node
..expandIsothenuria (HP:0030036)help
Term ID: 30036
Name: Isothenuria
Synonym:
Definition: Inability of the kidneys to produce either concentrated or dilute urine.
Comments:
Reference: HP:0030036
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal glomerular filtration rate (HP:0012212) help
..expandAbnormal renal tubular resorption (HP:0011038) help
..expandAbnormality of renal excretion (HP:0011036) help
..expandElevated alkaline phosphatase of renal origin (HP:0010680) help
..expandHematuria (HP:0000790) help
..expandHemolytic-uremic syndrome (HP:0005575) help
..expandImpaired urinary acidification (HP:0031033) help
..expandLow alkaline phosphatase of renal origin (HP:0010685) help
..expandNephritis (HP:0000123) help
..expandNephropathy (HP:0000112) help
..expandNephrotic syndrome (HP:0000100) help
..expandRenal insufficiency (HP:0000083) help
..expandRenal tubular dysfunction (HP:0000124) help
..expandRenovascular hypertension (HP:0100817) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030036HP:0030036Isothenuria0SLC4A1 CL E G H652111027OMIM:611590Renal tubular acidosis, distal, with hemolytic anemia.109


Genes (1) :SLC4A1

Diseases (1) :OMIM:611590
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.