Term ID: |
1563 |
Name: |
Fetal polyuria |
Synonym: |
Foetal polyuria |
Definition: |
Abnormally increased production of urine by the fetus resulting in polyhydramnios. |
Comments: |
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Reference: |
HP:0001563 |
Genes and Diseases: | | Child Nodes: | Sister Nodes: | ..Meconium stained amniotic fluid (HP:0012420)
| ..Oligohydramnios (HP:0001562)
| ..Polyhydramnios (HP:0001561)
| Input | HPO ID | HPO term | Distance | Gene | Gene id entrez | HGNC ID | DiseaseId | DiseaseName | Frequency | Onset | HGMD variants | ClinVar variants |
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HPO disease - gene - phenotype typical associations: | HPO disease - gene - phenotype less frequent non-typical associations: | HP:0001563 | HP:0001563 | Fetal polyuria | 0 | BSND CL E G H | 7809 | 16512 | OMIM:602522 | Bartter syndrome, type 4A, neonatal, with sensorineural deafness | . | | | 53 | | | HP:0001563 | HP:0001563 | Fetal polyuria | 0 | CLCNKA CL E G H | 1187 | 2026 | OMIM:613090 | Bartter syndrome, type 4B, neonatal, with sensorineural deafness | . | | | 9 | | | HP:0001563 | HP:0001563 | Fetal polyuria | 0 | CLCNKB CL E G H | 1188 | 2027 | OMIM:613090 | Bartter syndrome, type 4B, neonatal, with sensorineural deafness | . | | | 27 | | | HP:0001563 | HP:0001563 | Fetal polyuria | 0 | FGF20 CL E G H | 26281 | 3677 | ORPHA:1848 | Renal agenesis, bilateral | HP:0040282 - Frequent | | | 2 | | | HP:0001563 | HP:0001563 | Fetal polyuria | 0 | GFRA1 CL E G H | 2674 | 4243 | ORPHA:1848 | Renal agenesis, bilateral | HP:0040282 - Frequent | | | 1 | | | HP:0001563 | HP:0001563 | Fetal polyuria | 0 | GREB1L CL E G H | 80000 | 31042 | ORPHA:1848 | Renal agenesis, bilateral | HP:0040282 - Frequent | | | | | | HP:0001563 | HP:0001563 | Fetal polyuria | 0 | ITGA8 CL E G H | 8516 | 6144 | ORPHA:1848 | Renal agenesis, bilateral | HP:0040282 - Frequent | | | 4 | | | HP:0001563 | HP:0001563 | Fetal polyuria | 0 | KCNJ1 CL E G H | 3758 | 6255 | OMIM:241200 | Bartter syndrome, antenatal, type 2 | . | | | 51 | | | HP:0001563 | HP:0001563 | Fetal polyuria | 0 | MAGED2 CL E G H | 10916 | 16353 | OMIM:300971 | Bartter syndrome, type 5, antenatal, transient | . | | | 6 | | | HP:0001563 | HP:0001563 | Fetal polyuria | 0 | RET CL E G H | 5979 | 9967 | ORPHA:1848 | Renal agenesis, bilateral | HP:0040282 - Frequent | | | 572 | | | HP:0001563 | HP:0001563 | Fetal polyuria | 0 | SLC12A1 CL E G H | 6557 | 10910 | OMIM:601678 | Bartter syndrome, type 1, antenatal | . | | | 75 | | | HP:0001563 | HP:0001563 | Fetal polyuria | 0 | WNT9B CL E G H | 7484 | 12779 | ORPHA:1848 | Renal agenesis, bilateral | HP:0040282 - Frequent | | | | | |
Genes (12) :BSND CLCNKA CLCNKB FGF20 GFRA1 GREB1L ITGA8 KCNJ1 MAGED2 RET SLC12A1 WNT9B
Diseases (6) :OMIM:602522 OMIM:613090 ORPHA:1848 OMIM:241200 OMIM:300971 OMIM:601678 |
Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.
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