Human Phenotype Ontology 
Grandparent Node:
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Feeding difficulties (HP:0011968)help
Parent Node:
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Feeding difficulties in infancy (HP:0008872)help
..Starting node
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Poor suck (HP:0002033)help
Term ID: 2033
Name: Poor suck
Synonym: Poor suck; Poor sucking
Definition: An inadequate sucking reflex, resulting in the difficult of newborns to be breast-fed.
Comments:
Reference: HP:0002033
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandGastrojejunal tube feeding in infancy (HP:0030884) help
..expandGastrostomy tube feeding in infancy (HP:0011471) help
..expandNasal regurgitation (HP:0011469) help
..expandNasogastric tube feeding in infancy (HP:0011470) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0002033HP:0002033Poor suck0ACTA1 CL E G H582020ORPHA1217272129102610
HP:0002033HP:0002033Poor suck0AGRN CL E G H37579098914ORPHA118942329103320
HP:0002033HP:0002033Poor suck0ATP7A CL E G H538198ORPHA1357607869300011
HP:0002033HP:0002033Poor suck0BRAF CL E G H673613706Noonan syndrome 7613706C3150970OMIM1684901097164757
HP:0002033HP:0002033Poor suck0CHAT CL E G H110398914ORPHA1773741912118490
HP:0002033HP:0002033Poor suck0CHAT CL E G H1103254210Familial infantile myasthenia254210C0393929OMIM1773741912118490
HP:0002033HP:0002033Poor suck0CHRNA1 CL E G H1134608930Congenital myasthenic syndrome 1B, fast-channel608930C1837122OMIM1362361955100690
HP:0002033HP:0002033Poor suck0CHRNE CL E G H1145605809Myasthenic syndrome, congenital, 4a, slow-channel605809C1853949OMIM11383871966100725
HP:0002033HP:0002033Poor suck0CNTN1 CL E G H1272612540Myopathy, congenital, compton-north612540C2675527OMIM122502171600016
HP:0002033HP:0002033Poor suck0COL13A1 CL E G H130598914ORPHA13682190120350
HP:0002033HP:0002033Poor suck0COLQ CL E G H829298915ORPHA1702622226603033
HP:0002033HP:0002033Poor suck0DHCR7 CL E G H1717270400Smith-Lemli-Opitz syndrome270400C0175694OMIM12183762860602858
HP:0002033HP:0002033Poor suck0HACD1 CL E G H92002020ORPHA11339639610467
HP:0002033HP:0002033Poor suck0HADHA CL E G H3030746Apert like polydactyly syndromeORPHA1713024801600890
HP:0002033HP:0002033Poor suck0HADHB CL E G H3032746Apert like polydactyly syndromeORPHA1671484803143450
HP:0002033HP:0002033Poor suck0HERC2 CL E G H8924176270Prader-Willi syndrome176270C0032897OMIM164824868605837
HP:0002033HP:0002033Poor suck0HRAS CL E G H3265218040Costello syndrome218040C0587248OMIM1342955173190020
HP:0002033HP:0002033Poor suck0HTRA2 CL E G H274296172483-methylglutaconic aciduria, type VIII617248C4310650OMIM1147714348606441
HP:0002033HP:0002033Poor suck0IPW CL E G H3653176270Prader-Willi syndrome176270C0032897OMIM13116109601491
HP:0002033HP:0002033Poor suck0ITGA7 CL E G H36792020ORPHA1103706143600536
HP:0002033HP:0002033Poor suck0LAMB2 CL E G H391398915ORPHA11273686487150325
HP:0002033HP:0002033Poor suck0MAGEL2 CL E G H54551176270Prader-Willi syndrome176270C0032897OMIM1204536814605283
HP:0002033HP:0002033Poor suck0MAP3K20 CL E G H517762020ORPHA173617797609479
HP:0002033HP:0002033Poor suck0MKRN3 CL E G H7681176270Prader-Willi syndrome176270C0032897OMIM1323317114603856
HP:0002033HP:0002033Poor suck0MKRN3-AS1 CL E G H10108176270Prader-Willi syndrome176270C0032897OMIM112910603857
HP:0002033HP:0002033Poor suck0MYL2 CL E G H46332020ORPHA1672827583160781
HP:0002033HP:0002033Poor suck0MYO9A CL E G H464998914ORPHA16957608604875
HP:0002033HP:0002033Poor suck0NDN CL E G H4692176270Prader-Willi syndrome176270C0032897OMIM123147675602117
HP:0002033HP:0002033Poor suck0NPAP1 CL E G H23742176270Prader-Willi syndrome176270C0032897OMIM13431190610922
HP:0002033HP:0002033Poor suck0PEX2 CL E G H5828614866Peroxisome biogenesis disorder 5a (zellweger)614866C3553940OMIM1182089717170993
HP:0002033HP:0002033Poor suck0PEX5 CL E G H5830214110Peroxisome biogenesis disorder 2a (zellweger)214110C1859228OMIM1142809719600414
HP:0002033HP:0002033Poor suck0PLAA CL E G H9373617527NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES617527C4479631OMIM13849043603873
HP:0002033HP:0002033Poor suck0PQBP1 CL E G H10084309500Renpenning syndrome 1309500C0796135OMIM1222289330300463
HP:0002033HP:0002033Poor suck0PTS CL E G H58052616406-pyruvoyl-tetrahydropterin synthase deficiency261640C0878676OMIM1112989689612719
HP:0002033HP:0002033Poor suck0PWAR1 CL E G H145624176270Prader-Willi syndrome176270C0032897OMIM131130089600161
HP:0002033HP:0002033Poor suck0PWRN1 CL E G H791114176270Prader-Willi syndrome176270C0032897OMIM132233235611215
HP:0002033HP:0002033Poor suck0RARS2 CL E G H57038611523Pontocerebellar hypoplasia type 6611523C1969084OMIM13721621406611524
HP:0002033HP:0002033Poor suck0RHBDF2 CL E G H796512198ORPHA1414220788614404
HP:0002033HP:0002033Poor suck0SELENON CL E G H571902020ORPHA16335415999606210
HP:0002033HP:0002033Poor suck0SIK1 CL E G H1500941935ORPHA1741411142605705
HP:0002033HP:0002033Poor suck0SLC18A3 CL E G H657298914ORPHA168910936600336
HP:0002033HP:0002033Poor suck0SLC25A1 CL E G H657698914ORPHA12442910979190315
HP:0002033HP:0002033Poor suck0SLC25A22 CL E G H797511935ORPHA11031719954609302
HP:0002033HP:0002033Poor suck0SLC52A1 CL E G H55065615026Vitamin B2 deficiency615026C0035528OMIM136230225607883
HP:0002033HP:0002033Poor suck0SLC5A7 CL E G H6048298914ORPHA12016914025608761
HP:0002033HP:0002033Poor suck0SLC5A7 CL E G H60482617143Myasthenic syndrome, congenital, 20, presynaptic617143C4310694OMIM12016914025608761
HP:0002033HP:0002033Poor suck0SNAP25 CL E G H661698914ORPHA176411132600322
HP:0002033HP:0002033Poor suck0SNORD115-1 CL E G H338433176270Prader-Willi syndrome176270C0032897OMIM131333020609837
HP:0002033HP:0002033Poor suck0SNORD116-1 CL E G H100033413176270Prader-Willi syndrome176270C0032897OMIM131433067605436
HP:0002033HP:0002033Poor suck0SNRPN CL E G H6638176270Prader-Willi syndrome176270C0032897OMIM12538511164182279
HP:0002033HP:0002033Poor suck0SYT2 CL E G H12783398914ORPHA133911510600104
HP:0002033HP:0002033Poor suck0TALDO1 CL E G H6888606003Deficiency of transaldolase606003C1291329OMIM1108811559602063
HP:0002033HP:0002033Poor suck0TBC1D24 CL E G H5746579500ORPHA15656429203613577
HP:0002033HP:0002033Poor suck0TPM2 CL E G H71692020ORPHA14019912011190990
HP:0002033HP:0002033Poor suck0TPM3 CL E G H71702020ORPHA12822512012191030
HP:0002033HP:0002033Poor suck0TSEN54 CL E G H283989277470Pontocerebellar hypoplasia type 2A277470C1848526OMIM12117627561608755
HP:0002033HP:0002033Poor suck0VAMP1 CL E G H684398914ORPHA166412642185880
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0002033HP:0002033Poor suck0HRAS CL E G H32653071ORPHA0342955173190020
HP:0002033HP:0002033Poor suck0MT-TE CL E G H4556254864ORPHA07479590025
HP:0002033HP:0002033Poor suck0TRMU CL E G H55687254864ORPHA02329625481610230


Genes (57) :ACTA1 AGRN ATP7A BRAF CHAT CHRNA1 CHRNE CNTN1 COL13A1 COLQ DHCR7 HACD1 HADHA HADHB HERC2 HRAS HTRA2 IPW ITGA7 LAMB2 MAGEL2 MAP3K20 MKRN3 MKRN3-AS1 MYL2 MYO9A NDN NPAP1 PEX2 PEX5 PLAA PQBP1 PTS PWAR1 PWRN1 RARS2 RHBDF2 SELENON SIK1 SLC18A3 SLC25A1 SLC25A22 SLC52A1 SLC5A7 SNAP25 SNORD115-1 SNORD116-1 SNRPN SYT2 TALDO1 TBC1D24 TPM2 TPM3 TRMU TRNE TSEN54 VAMP1

Diseases (29) :2020 98914 198 613706 254210 608930 605809 612540 98915 270400 746 176270 3071 218040 617248 614866 214110 617527 309500 261640 611523 2198 1935 615026 617143 606003 79500 254864 277470
 

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