| Human Phenotype
Ontology
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Grandparent Node:
 Mode of inheritance (HP:0000005) | Parent Node:
obsolete Gonosomal inheritance (HP:0010985) | ..Starting node
..Y-linked inheritance (HP:0001450)
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| Term ID: |
1450 |
| Name: |
Y-linked inheritance |
| Synonym: |
monoallelic_Y_hemizygous; Y-linked |
| Definition: |
A mode of inheritance that is observed for traits related to a gene encoded on the Y chromosome. |
| Comments: |
|
| Reference: |
HP:0001450 |
| Genes and Diseases: | |
Child Nodes: |
Sister Nodes: | ..X-linked inheritance (HP:0001417)
| | Input | HPO ID | HPO term | Distance | Gene | Gene id entrez | HGNC ID | DiseaseId | DiseaseName | Frequency | Onset | HGMD variants | ClinVar variants |
|---|
HPO disease - gene - phenotype typical associations: |
HPO disease - gene - phenotype less frequent non-typical associations: | | HP:0001450 | HP:0001450 | Y-linked inheritance | 0 | BPY2 CL E G H | 9083 | 13508 | OMIM:415000 | SPERMATOGENIC FAILURE, NONOBSTRUCTIVE, Y-LINKED | . | | | | | | | HP:0001450 | HP:0001450 | Y-linked inheritance | 0 | CDY1 CL E G H | 9085 | 1809 | OMIM:415000 | SPERMATOGENIC FAILURE, NONOBSTRUCTIVE, Y-LINKED | . | | | | | | | HP:0001450 | HP:0001450 | Y-linked inheritance | 0 | CDY2A CL E G H | 9426 | 1810 | OMIM:415000 | SPERMATOGENIC FAILURE, NONOBSTRUCTIVE, Y-LINKED | . | | | | | | | HP:0001450 | HP:0001450 | Y-linked inheritance | 0 | DAZ1 CL E G H | 1617 | 2682 | OMIM:415000 | SPERMATOGENIC FAILURE, NONOBSTRUCTIVE, Y-LINKED | . | | | | | | | HP:0001450 | HP:0001450 | Y-linked inheritance | 0 | DAZ2 CL E G H | 57055 | 15964 | OMIM:415000 | SPERMATOGENIC FAILURE, NONOBSTRUCTIVE, Y-LINKED | . | | | | | | | HP:0001450 | HP:0001450 | Y-linked inheritance | 0 | DAZ3 CL E G H | 57054 | 15965 | OMIM:415000 | SPERMATOGENIC FAILURE, NONOBSTRUCTIVE, Y-LINKED | . | | | | | | | HP:0001450 | HP:0001450 | Y-linked inheritance | 0 | DDX3Y CL E G H | 8653 | 2699 | OMIM:415000 | SPERMATOGENIC FAILURE, NONOBSTRUCTIVE, Y-LINKED | . | | | | | | | HP:0001450 | HP:0001450 | Y-linked inheritance | 0 | HSFY1 CL E G H | 86614 | 18568 | OMIM:415000 | SPERMATOGENIC FAILURE, NONOBSTRUCTIVE, Y-LINKED | . | | | 1 | | | | HP:0001450 | HP:0001450 | Y-linked inheritance | 0 | KDM5D CL E G H | 8284 | 11115 | OMIM:415000 | SPERMATOGENIC FAILURE, NONOBSTRUCTIVE, Y-LINKED | . | | | | | | | HP:0001450 | HP:0001450 | Y-linked inheritance | 0 | PRY CL E G H | 9081 | 14024 | OMIM:415000 | SPERMATOGENIC FAILURE, NONOBSTRUCTIVE, Y-LINKED | . | | | | | | | HP:0001450 | HP:0001450 | Y-linked inheritance | 0 | PRY2 CL E G H | 442862 | 21504 | OMIM:415000 | SPERMATOGENIC FAILURE, NONOBSTRUCTIVE, Y-LINKED | . | | | 5 | | | | HP:0001450 | HP:0001450 | Y-linked inheritance | 0 | RBMY1A1 CL E G H | 5940 | 9912 | OMIM:415000 | SPERMATOGENIC FAILURE, NONOBSTRUCTIVE, Y-LINKED | . | | | | | | | HP:0001450 | HP:0001450 | Y-linked inheritance | 0 | RPS4Y2 CL E G H | 140032 | 18501 | OMIM:415000 | SPERMATOGENIC FAILURE, NONOBSTRUCTIVE, Y-LINKED | . | | | | | | | HP:0001450 | HP:0001450 | Y-linked inheritance | 0 | SRY CL E G H | 6736 | 11311 | OMIM:400044 | 46XY sex reversal 1 | | | | 23 | | | | HP:0001450 | HP:0001450 | Y-linked inheritance | 0 | TBL1Y CL E G H | 90665 | 18502 | OMIM:400047 | DEAFNESS, Y-LINKED 2 | | | | | | | | HP:0001450 | HP:0001450 | Y-linked inheritance | 0 | USP9Y CL E G H | 8287 | 12633 | OMIM:415000 | SPERMATOGENIC FAILURE, NONOBSTRUCTIVE, Y-LINKED | . | | | 2 | | | | HP:0001450 | HP:0001450 | Y-linked inheritance | 0 | VCY CL E G H | 9084 | 12668 | OMIM:415000 | SPERMATOGENIC FAILURE, NONOBSTRUCTIVE, Y-LINKED | . | | | 2 | | |
Genes (17) :BPY2 CDY1 CDY2A DAZ1 DAZ2 DAZ3 DDX3Y HSFY1 KDM5D PRY PRY2 RBMY1A1 RPS4Y2 SRY TBL1Y USP9Y VCY
Diseases (3) :OMIM:415000 OMIM:400044 OMIM:400047 |
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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