Human Phenotype Ontology 
Grandparent Node:
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Neoplasm of the thyroid gland (HP:0100031)help
Parent Node:
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Thyroid carcinoma (HP:0002890)help
..Starting node
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Follicular thyroid carcinoma (HP:0006731)help
Term ID: 6731
Name: Follicular thyroid carcinoma
Synonym:
Definition: The presence of an follicular adenocarcinoma of the thyroid gland.
Comments:
Reference: HP:0006731
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAnaplastic thyroid carcinoma (HP:0011779) help
..expandMedullary thyroid carcinoma (HP:0002865) help
..expandNon-medullary thyroid carcinoma (HP:0040198) help
..expandPapillary thyroid carcinoma (HP:0002895) 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:0006731HP:0006731Follicular thyroid carcinoma0AKT1 CL E G H207391ORPHA:201Cowden syndromeHP:0040283 - Occasional54
HP:0006731HP:0006731Follicular thyroid carcinoma0FOXE1 CL E G H23043806ORPHA:319487Familial papillary or follicular thyroid carcinomaHP:0040281 - Very frequent9
HP:0006731HP:0006731Follicular thyroid carcinoma0HABP2 CL E G H30264798ORPHA:319487Familial papillary or follicular thyroid carcinomaHP:0040281 - Very frequent58
HP:0006731HP:0006731Follicular thyroid carcinoma0HRAS CL E G H32655173OMIM:188470Thyroid cancer, nonmedullary, 2.113
HP:0006731HP:0006731Follicular thyroid carcinoma0KLLN CL E G H10014474837212ORPHA:201Cowden syndromeHP:0040283 - Occasional1
HP:0006731HP:0006731Follicular thyroid carcinoma0MINPP1 CL E G H95627102ORPHA:319487Familial papillary or follicular thyroid carcinomaHP:0040281 - Very frequent3
HP:0006731HP:0006731Follicular thyroid carcinoma0MINPP1 CL E G H95627102OMIM:188470Thyroid cancer, nonmedullary, 2.3
HP:0006731HP:0006731Follicular thyroid carcinoma0NRAS CL E G H48937989OMIM:188470Thyroid cancer, nonmedullary, 2.102
HP:0006731HP:0006731Follicular thyroid carcinoma0PDE11A CL E G H509408773ORPHA:1359Carney complex13
HP:0006731HP:0006731Follicular thyroid carcinoma0PIK3CA CL E G H52908975ORPHA:201Cowden syndromeHP:0040283 - Occasional162
HP:0006731HP:0006731Follicular thyroid carcinoma0PRKAR1A CL E G H55739388ORPHA:1359Carney complex134
HP:0006731HP:0006731Follicular thyroid carcinoma0PTEN CL E G H57289588ORPHA:201Cowden syndromeHP:0040283 - Occasional948
HP:0006731HP:0006731Follicular thyroid carcinoma0SDHB CL E G H639010681ORPHA:201Cowden syndromeHP:0040283 - Occasional237
HP:0006731HP:0006731Follicular thyroid carcinoma0SDHC CL E G H639110682ORPHA:201Cowden syndromeHP:0040283 - Occasional147
HP:0006731HP:0006731Follicular thyroid carcinoma0SDHD CL E G H639210683ORPHA:201Cowden syndromeHP:0040283 - Occasional129
HP:0006731HP:0006731Follicular thyroid carcinoma0SEC23B CL E G H1048310702ORPHA:201Cowden syndromeHP:0040283 - Occasional60
HP:0006731HP:0006731Follicular thyroid carcinoma0SRGAP1 CL E G H5752217382OMIM:188470Thyroid cancer, nonmedullary, 2.3
HP:0006731HP:0006731Follicular thyroid carcinoma0USF3 CL E G H20571730494ORPHA:201Cowden syndromeHP:0040283 - Occasional1


Genes (17) :AKT1 FOXE1 HABP2 HRAS KLLN MINPP1 NRAS PDE11A PIK3CA PRKAR1A PTEN SDHB SDHC SDHD SEC23B SRGAP1 USF3

Diseases (4) :ORPHA:201 ORPHA:319487 OMIM:188470 ORPHA:1359
 

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