Human Phenotype Ontology 
Grandparent Node:
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Abnormal hand morphology (HP:0005922)help
Grandparent Node:
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Aplasia/Hypoplasia of fingers (HP:0006265)help
Grandparent Node:
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Short digit (HP:0011927)help
Parent Node:
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Aplasia/Hypoplasia of the 5th finger (HP:0006262)help
Parent Node:
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Short finger (HP:0009381)help
..Starting node
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Short 5th finger (HP:0009237)help
Term ID: 9237
Name: Short 5th finger
Synonym: Fifth finger brachydactyly; Hypoplastic phalanges of the little finger; Hypoplastic/small 5th finger; Hypoplastic/small little finger; Short 5th finger; Short fifth finger; Short fifth fingers; Short little finger; Short phalanges of the little finger; Short pinkie finger; Short pinky finger
Definition: Hypoplasia (congenital reduction in size) of the fifth finger, also known as the little finger.
Comments:
Reference: HP:0009237
Genes and Diseases:
 
       Child Nodes:
........expandShort middle phalanx of the 5th finger (HP:0004220) help
........expandShort distal phalanx of the 5th finger (HP:0004227) help
........expandShort proximal phalanx of the 5th finger (HP:0009226) help

 Sister Nodes: 
..expandShort 2nd finger (HP:0009536) help
..expandShort 3rd finger (HP:0009461) help
..expandShort 4th finger (HP:0009280) help
..expandShort distal phalanx of finger (HP:0009882) help
..expandShort middle phalanx of finger (HP:0005819) help
..expandShort proximal phalanx of finger (HP:0010241) help
..expandShort thumb (HP:0009778) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0009237HP:0009237Short 5th finger0CUL7 CL E G H9820273750Three M syndrome 1273750C1848862OMIM18524821024609577
HP:0009237HP:0009237Short 5th finger0GJA1 CL E G H2697186100Syndactyly type 3186100C1861366OMIM11091414274121014
HP:0009237HP:0009237Short 5th finger0HOXA13 CL E G H3209140000Hand foot uterus syndrome140000C1841679OMIM130635102142959
HP:0009237HP:0009237Short 5th finger0KDM6A CL E G H74032322ORPHA18131112637300128
HP:0009237HP:0009237Short 5th finger0KDM6A CL E G H7403147920Kabuki syndrome 1147920CN030661OMIM18131112637300128
HP:0009237HP:0009237Short 5th finger0KMT2D CL E G H80852322ORPHA171213507133602113
HP:0009237HP:0009237Short 5th finger0KMT2D CL E G H8085147920Kabuki syndrome 1147920CN030661OMIM171213507133602113
HP:0009237HP:0009237Short 5th finger0MASP1 CL E G H5648257920Michels syndrome257920C0796059OMIM1221226901600521
HP:0009237HP:0009237Short 5th finger0MEIS2 CL E G H4212600987Cleft palate, cardiac defects, and mental retardation600987C1832950OMIM123577001601740
HP:0009237HP:0009237Short 5th finger0OBSL1 CL E G H23363612921Three M syndrome 2612921C2752041OMIM13533129092610991
HP:0009237HP:0009237Short 5th finger0PUF60 CL E G H22827615583Verheij syndrome615583C3810023OMIM13212917042604819
HP:0009237HP:0009237Short 5th finger0RAP1A CL E G H59062322ORPHA12209855179520
HP:0009237HP:0009237Short 5th finger0RAP1B CL E G H59082322ORPHA11199857179530
HP:0009237HP:0009237Short 5th finger0TBC1D24 CL E G H5746579500ORPHA15656429203613577
HP:0009237HP:0009237Short 5th finger0ZDHHC15 CL E G H158866300577Mental retardation 91, X-linked300577C1845142OMIM1117520342300576
HP:0009237HP:0009237Short 5th finger1CUL7 CL E G H9820273750Three M syndrome 1273750C1848862OMIM18524821024609577
HP:0009237HP:0009237Short 5th finger1GJA1 CL E G H2697186100Syndactyly type 3186100C1861366OMIM11091414274121014
HP:0009237HP:0009237Short 5th finger1HOXA13 CL E G H3209140000Hand foot uterus syndrome140000C1841679OMIM130635102142959
HP:0009237HP:0009237Short 5th finger1KDM6A CL E G H74032322ORPHA18131112637300128
HP:0009237HP:0009237Short 5th finger1KDM6A CL E G H7403147920Kabuki syndrome 1147920CN030661OMIM18131112637300128
HP:0009237HP:0009237Short 5th finger1KMT2D CL E G H80852322ORPHA171213507133602113
HP:0009237HP:0009237Short 5th finger1KMT2D CL E G H8085147920Kabuki syndrome 1147920CN030661OMIM171213507133602113
HP:0009237HP:0009237Short 5th finger1MASP1 CL E G H5648257920Michels syndrome257920C0796059OMIM1221226901600521
HP:0009237HP:0009237Short 5th finger1MEIS2 CL E G H4212600987Cleft palate, cardiac defects, and mental retardation600987C1832950OMIM123577001601740
HP:0009237HP:0009237Short 5th finger1OBSL1 CL E G H23363612921Three M syndrome 2612921C2752041OMIM13533129092610991
HP:0009237HP:0009237Short 5th finger1PUF60 CL E G H22827615583Verheij syndrome615583C3810023OMIM13212917042604819
HP:0009237HP:0009237Short 5th finger1RAP1A CL E G H59062322ORPHA12209855179520
HP:0009237HP:0009237Short 5th finger1RAP1B CL E G H59082322ORPHA11199857179530
HP:0009237HP:0009237Short 5th finger1TBC1D24 CL E G H5746579500ORPHA15656429203613577
HP:0009237HP:0009237Short 5th finger1ZDHHC15 CL E G H158866300577Mental retardation 91, X-linked300577C1845142OMIM1117520342300576
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0009237HP:0009237Short 5th finger0FGD1 CL E G H2245305400Aarskog syndrome305400C0175701OMIM0512763663300546
HP:0009237HP:0009237Short 5th finger0KDM6A CL E G H7403300867Kabuki syndrome 2300867C3275495OMIM08131112637300128
HP:0009237HP:0009237Short 5th finger0SMC3 CL E G H9126610759Cornelia de Lange syndrome 3610759C1853099OMIM0282132468606062
HP:0009237HP:0009237Short 5th finger1FGD1 CL E G H2245305400Aarskog syndrome305400C0175701OMIM0512763663300546
HP:0009237HP:0009237Short 5th finger1KDM6A CL E G H7403300867Kabuki syndrome 2300867C3275495OMIM08131112637300128
HP:0009237HP:0009237Short 5th finger1SMC3 CL E G H9126610759Cornelia de Lange syndrome 3610759C1853099OMIM0282132468606062


Genes (31) :ARID1B BMP2 BMPR1B COL2A1 CUL7 DVL1 DVL3 FGD1 GATA1 GDF5 GJA1 H19 HOXA13 HOXD13 IGF2 KDM6A KMT2D MASP1 MEIS2 OBSL1 PUF60 RAP1A RAP1B RBBP8 ROR2 RUNX2 SMC3 TBC1D24 TFAP2B WNT5A ZDHHC15

Diseases (33) :273750 305400 186100 140000 2322 147920 300867 257920 600987 612921 615583 610759 79500 300577 135900 93396 112600 616849 271700 180700 190685 63442 615072 164200 180860 93409 186000 508488 251255 268310 119600 156510 46627
 

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