Human Phenotype Ontology 
Grandparent Node:
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Syndactyly (HP:0001159)help
Parent Node:
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Finger syndactyly (HP:0006101)help
..Starting node
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2-3 finger syndactyly (HP:0001233)help
Term ID: 1233
Name: 2-3 finger syndactyly
Synonym: Syndactyly 2nd-3rd fingers; Syndactyly, 2-3 finger; Webbed 2nd-3rd fingers
Definition: Syndactyly with fusion of fingers two and three.
Comments:
Reference: HP:0001233
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expand1-2 finger syndactyly (HP:0010704) help
..expand1-3 finger syndactyly (HP:0010706) help
..expand1-4 finger syndactyly (HP:0010707) help
..expand1-5 finger syndactyly (HP:0010708) help
..expand2-4 finger syndactyly (HP:0010709) help
..expand2-5 finger syndactyly (HP:0010692) help
..expand3-4 finger syndactyly (HP:0006097) help
..expand3-5 finger syndactyly (HP:0010710) help
..expand4-5 finger syndactyly (HP:0010705) help
..expandCutaneous finger syndactyly (HP:0010554) help
..expandOsseous finger syndactyly (HP:0010492) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0001233HP:00012332-3 finger syndactyly0FGF10 CL E G H2255149730Levy-Hollister syndrome149730C0265269OMIM116473666602115
HP:0001233HP:00012332-3 finger syndactyly0FGFR2 CL E G H2263149730Levy-Hollister syndrome149730C0265269OMIM11593363689176943
HP:0001233HP:00012332-3 finger syndactyly0FGFR3 CL E G H2261149730Levy-Hollister syndrome149730C0265269OMIM1774313690134934
HP:0001233HP:00012332-3 finger syndactyly0GPC3 CL E G H2719312870Simpson-Golabi-Behmel syndrome312870C0796154OMIM1985264451300037
HP:0001233HP:00012332-3 finger syndactyly0GPC4 CL E G H2239312870Simpson-Golabi-Behmel syndrome312870C0796154OMIM151964452300168
HP:0001233HP:00012332-3 finger syndactyly0LRP4 CL E G H40383152Kuster syndromeORPHA1343756696604270
HP:0001233HP:00012332-3 finger syndactyly0PITX1 CL E G H5307186550Liebenberg syndrome186550C1861313OMIM118349004602149
HP:0001233HP:00012332-3 finger syndactyly0SOST CL E G H509643152Kuster syndromeORPHA1177013771605740
HP:0001233HP:00012332-3 finger syndactyly0SOST CL E G H50964269500Sclerosteosis 1269500CN032489OMIM1177013771605740
HP:0001233HP:00012332-3 finger syndactyly0WDPCP CL E G H510571338ORPHA1817628027613580
HP:0001233HP:00012332-3 finger syndactyly0WDPCP CL E G H51057217085Orstavik Lindemann Solberg syndrome217085C1857587OMIM1817628027613580
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (9) :FGF10 FGFR2 FGFR3 GPC3 GPC4 LRP4 PITX1 SOST WDPCP

Diseases (7) :149730 312870 3152 186550 269500 1338 217085
 

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