| Human Phenotype
Ontology
|
..Starting node
.. Third trimester onset (HP:0034197)
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| Term ID: |
34197 |
| Name: |
Third trimester onset |
| Synonym: |
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| Definition: |
This term refers to a phenotypic feature that was first observed prior to birth during the third trimester, which is defined as 28 weeks and zero days (28+0) of gestation and beyond. |
| Comments: |
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| Reference: |
HP:0034197 |
| Genes and Diseases: | |
Child Nodes: |
Sister Nodes: | | 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:0034197 | HP:0034197 | Third trimester onset | 0 | ALPK3 CL E G H | 57538 | 17574 | OMIM:618052 | Cardiomyopathy, familial hypertrophic 27 | | | | 89 | | | | HP:0034197 | HP:0034197 | Third trimester onset | 0 | FANCB CL E G H | 2187 | 3583 | OMIM:314390 | VACTERL association, X-linked | | | | 58 | | | | HP:0034197 | HP:0034197 | Third trimester onset | 0 | GINS1 CL E G H | 9837 | 28980 | OMIM:617827 | Immunodeficiency 55 | | | | | | | | HP:0034197 | HP:0034197 | Third trimester onset | 0 | KMT2B CL E G H | 9757 | 15840 | OMIM:619934 | | | | | 11 | | | | HP:0034197 | HP:0034197 | Third trimester onset | 0 | MDFIC CL E G H | 29969 | 28870 | OMIM:620014 | | | | | | | | | HP:0034197 | HP:0034197 | Third trimester onset | 0 | NUP155 CL E G H | 9631 | 8063 | OMIM:615770 | Atrial fibrillation, familial, 15 | | | | 1 | | | | HP:0034197 | HP:0034197 | Third trimester onset | 0 | PLG CL E G H | 5340 | 9071 | OMIM:217090 | Plasminogen deficiency, type iligneous conjunctivitis, included | | | | 11 | | | | HP:0034197 | HP:0034197 | Third trimester onset | 0 | PYCR1 CL E G H | 5831 | 9721 | OMIM:612940 | Cutis laxa, autosomal recessive, type IIB | | | | 53 | | | | HP:0034197 | HP:0034197 | Third trimester onset | 0 | SDHA CL E G H | 6389 | 10680 | OMIM:613642 | Cardiomyopathy, dilated, 1gg | | | | 304 | | | | HP:0034197 | HP:0034197 | Third trimester onset | 0 | SHQ1 CL E G H | 55164 | 25543 | OMIM:619922 | | | | | | | | | HP:0034197 | HP:0034197 | Third trimester onset | 0 | SNAP25 CL E G H | 6616 | 11132 | OMIM:616330 | Myasthenic syndrome, congenital, 18 | | | | 2 | | | | HP:0034197 | HP:0034197 | Third trimester onset | 0 | TNFRSF11A CL E G H | 8792 | 11908 | OMIM:602080 | Paget disease of bone 2, early-onset | | | | 72 | | | | HP:0034197 | HP:0034197 | Third trimester onset | 0 | ZIC3 CL E G H | 7547 | 12874 | OMIM:314390 | VACTERL association, X-linked | | | | 39 | | | | HP:0034197 | HP:0034197 | Third trimester onset | 0 | ZMPSTE24 CL E G H | 10269 | 12877 | OMIM:275210 | Restrictive dermopathy, lethal | | | | 83 | | |
Genes (14) :ALPK3 FANCB GINS1 KMT2B MDFIC NUP155 PLG PYCR1 SDHA SHQ1 SNAP25 TNFRSF11A ZIC3 ZMPSTE24
Diseases (13) :OMIM:618052 OMIM:314390 OMIM:617827 OMIM:619934 OMIM:620014 OMIM:615770 OMIM:217090 OMIM:612940 OMIM:613642 OMIM:619922 OMIM:616330 OMIM:602080 OMIM:275210 |
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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