Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the tongue (HP:0000157)help
Grandparent Node:
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Neoplasm of the oral cavity (HP:0100649)help
Parent Node:
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Neoplasm of the tongue (HP:0100648)help
..Starting node
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Hamartoma of tongue (HP:0011802)help
Term ID: 11802
Name: Hamartoma of tongue
Synonym: Lingual hamartoma
Definition: A benign (noncancerous) tumorlike malformation made up of an abnormal mixture of cells and tissues that originates in the tongue.
Comments:
Reference: HP:0011802
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandLipoma of the tongue (HP:0030815) help
..expandSquamous cell carcinoma of the tongue (HP:0030413) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0011802HP:0011802Hamartoma of tongue0C2CD3 CL E G H26005615948Orofaciodigital syndrome xiv615948C4014780OMIM135524564615944
HP:0011802HP:0011802Hamartoma of tongue0C2CD3 CL E G H26005615948Orofaciodigital syndrome xiv615948C4014780OMIM123824564615944
HP:0011802HP:0011802Hamartoma of tongue0CPLANE1 CL E G H652502754ORPHA1123925801614571
HP:0011802HP:0011802Hamartoma of tongue0CPLANE1 CL E G H652502754ORPHA182425801614571
HP:0011802HP:0011802Hamartoma of tongue0KIAA0753 CL E G H98512754ORPHA118429110617112
HP:0011802HP:0011802Hamartoma of tongue0KIAA0753 CL E G H98512754ORPHA112229110617112
HP:0011802HP:0011802Hamartoma of tongue0KIF7 CL E G H3746542754ORPHA181330497611254
HP:0011802HP:0011802Hamartoma of tongue0KIF7 CL E G H3746542754ORPHA154030497611254
HP:0011802HP:0011802Hamartoma of tongue0NEK1 CL E G H47502751Hunter Carpenter Macdonald syndromeORPHA14737744604588
HP:0011802HP:0011802Hamartoma of tongue0NEK1 CL E G H47502751Hunter Carpenter Macdonald syndromeORPHA14187744604588
HP:0011802HP:0011802Hamartoma of tongue0NEK1 CL E G H4750263520Short rib-polydactyly syndrome, Majewski type263520C0024507OMIM14737744604588
HP:0011802HP:0011802Hamartoma of tongue0NEK1 CL E G H4750263520Short rib-polydactyly syndrome, Majewski type263520C0024507OMIM14187744604588
HP:0011802HP:0011802Hamartoma of tongue0OFD1 CL E G H84812754ORPHA17232567300170
HP:0011802HP:0011802Hamartoma of tongue0OFD1 CL E G H84812750ORPHA17232567300170
HP:0011802HP:0011802Hamartoma of tongue0OFD1 CL E G H84812754ORPHA16472567300170
HP:0011802HP:0011802Hamartoma of tongue0OFD1 CL E G H84812750ORPHA16472567300170
HP:0011802HP:0011802Hamartoma of tongue0PDE6D CL E G H51472754ORPHA1578788602676
HP:0011802HP:0011802Hamartoma of tongue0PDE6D CL E G H51472754ORPHA1418788602676
HP:0011802HP:0011802Hamartoma of tongue0TCTN3 CL E G H261232754ORPHA125624519613847
HP:0011802HP:0011802Hamartoma of tongue0TCTN3 CL E G H261232754ORPHA114824519613847
HP:0011802HP:0011802Hamartoma of tongue0TCTN3 CL E G H26123258860Orofacial-digital syndrome IV258860C0406727OMIM125624519613847
HP:0011802HP:0011802Hamartoma of tongue0TCTN3 CL E G H26123258860Orofacial-digital syndrome IV258860C0406727OMIM114824519613847
HP:0011802HP:0011802Hamartoma of tongue0TMEM107 CL E G H84314617563OROFACIODIGITAL SYNDROME XVI617563C4539729OMIM116128128616183
HP:0011802HP:0011802Hamartoma of tongue0TMEM107 CL E G H84314617563OROFACIODIGITAL SYNDROME XVI617563C4539729OMIM110128128616183
HP:0011802HP:0011802Hamartoma of tongue0TMEM216 CL E G H512592754ORPHA116825018613277
HP:0011802HP:0011802Hamartoma of tongue0TMEM216 CL E G H512592754ORPHA115125018613277
HP:0011802HP:0011802Hamartoma of tongue0TMEM231 CL E G H795832752ORPHA129937234614949
HP:0011802HP:0011802Hamartoma of tongue0TMEM231 CL E G H795832752ORPHA120937234614949
HP:0011802HP:0011802Hamartoma of tongue0WDPCP CL E G H510571338ORPHA136728027613580
HP:0011802HP:0011802Hamartoma of tongue0WDPCP CL E G H510571338ORPHA127528027613580
HP:0011802HP:0011802Hamartoma of tongue0WDPCP CL E G H51057217085Orstavik Lindemann Solberg syndrome217085C1857587OMIM136728027613580
HP:0011802HP:0011802Hamartoma of tongue0WDPCP CL E G H51057217085Orstavik Lindemann Solberg syndrome217085C1857587OMIM127528027613580
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011802HP:0011802Hamartoma of tongue0DYNC2H1 CL E G H79659613091Short-rib thoracic dysplasia 3 with or without polydactyly613091C2751311OMIM013762962603297
HP:0011802HP:0011802Hamartoma of tongue0DYNC2H1 CL E G H79659613091Short-rib thoracic dysplasia 3 with or without polydactyly613091C2751311OMIM012032962603297
HP:0011802HP:0011802Hamartoma of tongue0EDN1 CL E G H1906137888ORPHA0523176131240
HP:0011802HP:0011802Hamartoma of tongue0EDN1 CL E G H1906137888ORPHA0513176131240
HP:0011802HP:0011802Hamartoma of tongue0GNAI3 CL E G H2773137888ORPHA0374387139370
HP:0011802HP:0011802Hamartoma of tongue0GNAI3 CL E G H2773137888ORPHA0364387139370
HP:0011802HP:0011802Hamartoma of tongue0INTU CL E G H27152617925SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY617925CN902090OMIM07929239610621
HP:0011802HP:0011802Hamartoma of tongue0INTU CL E G H27152617925SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY617925CN902090OMIM06129239610621
HP:0011802HP:0011802Hamartoma of tongue0PLCB4 CL E G H5332137888ORPHA02179059600810
HP:0011802HP:0011802Hamartoma of tongue0PLCB4 CL E G H5332137888ORPHA02149059600810


Genes (17) :C2CD3 CPLANE1 DYNC2H1 EDN1 GNAI3 INTU KIAA0753 KIF7 NEK1 OFD1 PDE6D PLCB4 TCTN3 TMEM107 TMEM216 TMEM231 WDPCP

Diseases (13) :615948 2754 613091 137888 617925 2751 263520 2750 258860 617563 2752 1338 217085
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.