Human Phenotype Ontology 
Grandparent Node:
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Abnormality of dental eruption (HP:0006292)help
Parent Node:
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Advanced eruption of teeth (HP:0006288)help
..Starting node
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Natal tooth (HP:0000695)help
Term ID: 695
Name: Natal tooth
Synonym: Born with teeth; Natal teeth; Neonatal teeth; Teeth present at birth
Definition: Erupted tooth or teeth at birth.
Comments:
Reference: HP:0000695
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandPremature eruption of permanent teeth (HP:0006337) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0000695HP:0000695Natal tooth0AMER1 CL E G H139285300373Osteopathia striata with cranial sclerosis300373C0432268OMIM14121926837300647
HP:0000695HP:0000695Natal tooth0BCL11B CL E G H64919617237Immunodeficiency 49617237C4310656OMIM1126513222606558
HP:0000695HP:0000695Natal tooth0CEP120 CL E G H153241616300Short-rib thoracic dysplasia 13 with or without polydactyly616300C4225378OMIM198726690613446
HP:0000695HP:0000695Natal tooth0DSP CL E G H1832609638Epidermolysis bullosa, lethal acantholytic609638C1864826OMIM130921793052125647
HP:0000695HP:0000695Natal tooth0EVC CL E G H2121225500Chondroectodermal dysplasia225500C0013903OMIM1846523497604831
HP:0000695HP:0000695Natal tooth0EVC2 CL E G H132884225500Chondroectodermal dysplasia225500C0013903OMIM17656719747607261
HP:0000695HP:0000695Natal tooth0FGFR2 CL E G H2263313855ORPHA11593363689176943
HP:0000695HP:0000695Natal tooth0FLNA CL E G H231699811ORPHA127114723754300017
HP:0000695HP:0000695Natal tooth0GLI3 CL E G H2737672Angiofollicular ganglionic hyperplasiaORPHA12445374319165240
HP:0000695HP:0000695Natal tooth0KRT17 CL E G H3872167210Pachyonychia congenita 2167210C1721007OMIM129506427148069
HP:0000695HP:0000695Natal tooth0LMNA CL E G H4000275210Lethal tight skin contracture syndrome275210C0406585OMIM157411526636150330
HP:0000695HP:0000695Natal tooth0MKS1 CL E G H54903249000Meckel syndrome type 1249000C3714506OMIM1523347121609883
HP:0000695HP:0000695Natal tooth0POLR3A CL E G H11128264090Neonatal pseudo-hydrocephalic progeroid syndrome264090C0406586OMIM19230630074614258
HP:0000695HP:0000695Natal tooth0PTH1R CL E G H574550945ORPHA1451009608168468
HP:0000695HP:0000695Natal tooth0SPECC1L CL E G H23384145420Brachycephalofrontonasal dysplasia145420C0796179OMIM1815629022614140
HP:0000695HP:0000695Natal tooth0ZMPSTE24 CL E G H10269275210Lethal tight skin contracture syndrome275210C0406585OMIM13413612877606480
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0000695HP:0000695Natal tooth0DSP CL E G H1832158687ORPHA030921793052125647
HP:0000695HP:0000695Natal tooth0EHMT1 CL E G H79813610253Chromosome 9q deletion syndrome610253C0795833OMIM09474624650607001
HP:0000695HP:0000695Natal tooth0FAM20C CL E G H56975259775Raine syndrome259775C1850106OMIM02813922140611061
HP:0000695HP:0000695Natal tooth0GLI3 CL E G H2737146510Pallister-Hall syndrome146510C0265220OMIM02445374319165240
HP:0000695HP:0000695Natal tooth0INTU CL E G H27152617925SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY617925CN902090OMIM0123229239610621
HP:0000695HP:0000695Natal tooth0JUP CL E G H3728158687ORPHA0485026207173325
HP:0000695HP:0000695Natal tooth0KDF1 CL E G H126695617337Ectodermal dysplasia 12, hypohidrotic/hair/tooth/nail type617337C4310616OMIM021626624616758
HP:0000695HP:0000695Natal tooth0KDM6A CL E G H7403300867Kabuki syndrome 2300867C3275495OMIM08131112637300128
HP:0000695HP:0000695Natal tooth0LMNA CL E G H40001662ORPHA057411526636150330
HP:0000695HP:0000695Natal tooth0NEK1 CL E G H47502751Hunter Carpenter Macdonald syndromeORPHA0303117744604588
HP:0000695HP:0000695Natal tooth0ZMPSTE24 CL E G H102691662ORPHA03413612877606480


Genes (23) :AMER1 BCL11B CEP120 DSP EHMT1 EVC EVC2 FAM20C FGFR2 FLNA GLI3 INTU JUP KDF1 KDM6A KRT17 LMNA MKS1 NEK1 POLR3A PTH1R SPECC1L ZMPSTE24

Diseases (23) :300373 617237 616300 158687 609638 610253 225500 259775 313855 99811 672 146510 617925 617337 300867 167210 1662 275210 249000 2751 264090 50945 145420
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.