Human Phenotype Ontology 
Grandparent Node:
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Growth delay (HP:0001510)help
Parent Node:
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Postnatal growth retardation (HP:0008897)help
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Mild postnatal growth retardation (HP:0001530)help
Term ID: 1530
Name: Mild postnatal growth retardation
Synonym: Mild growth deficiency; Postnatal onset of mild growth retardation
Definition: A mild degree of slow or limited growth after birth, being between two and three standard deviations below age- and sex-related norms.
Comments:
Reference: HP:0001530
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandModerate postnatal growth retardation (HP:0008855) help
..expandSevere postnatal growth retardation (HP:0008850) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0001530HP:0001530Mild postnatal growth retardation0ADAMTS3 CL E G H9508219ORPHA:2136Hennekam syndromeHP:0040281 - Very frequent1
HP:0001530HP:0001530Mild postnatal growth retardation0ANKRD55 CL E G H7972225681ORPHA:85408Rheumatoid factor-negative polyarticular juvenile idiopathic arthritisHP:0040283 - Occasional
HP:0001530HP:0001530Mild postnatal growth retardation0CCBE1 CL E G H14737229426OMIM:235510Hennekam lymphangiectasia-lymphedema syndrome.147
HP:0001530HP:0001530Mild postnatal growth retardation0CCBE1 CL E G H14737229426ORPHA:2136Hennekam syndromeHP:0040281 - Very frequent147
HP:0001530HP:0001530Mild postnatal growth retardation0CD247 CL E G H9191677ORPHA:85408Rheumatoid factor-negative polyarticular juvenile idiopathic arthritisHP:0040283 - Occasional8
HP:0001530HP:0001530Mild postnatal growth retardation0CDAN1 CL E G H1460591713OMIM:224120Anemia, congenital dyserythropoietic, type Ia.86
HP:0001530HP:0001530Mild postnatal growth retardation0ERCC6 CL E G H20743438ORPHA:90324Cockayne syndrome type 3HP:0040283 - Occasional199
HP:0001530HP:0001530Mild postnatal growth retardation0ERCC8 CL E G H11613439ORPHA:90324Cockayne syndrome type 3HP:0040283 - Occasional55
HP:0001530HP:0001530Mild postnatal growth retardation0FAT4 CL E G H7963323109ORPHA:2136Hennekam syndromeHP:0040281 - Very frequent114
HP:0001530HP:0001530Mild postnatal growth retardation0IGFALS CL E G H34835468OMIM:615961ACID-LABILE SUBUNIT DEFICIENCY; ACLSD53
HP:0001530HP:0001530Mild postnatal growth retardation0IL2RA CL E G H35596008ORPHA:85408Rheumatoid factor-negative polyarticular juvenile idiopathic arthritisHP:0040283 - Occasional65
HP:0001530HP:0001530Mild postnatal growth retardation0IL2RB CL E G H35606009ORPHA:85408Rheumatoid factor-negative polyarticular juvenile idiopathic arthritisHP:0040283 - Occasional
HP:0001530HP:0001530Mild postnatal growth retardation0PRKAR1A CL E G H55739388OMIM:101800Acrodysostosis 1, with or without hormone resistance.134
HP:0001530HP:0001530Mild postnatal growth retardation0PTPN2 CL E G H57719650ORPHA:85408Rheumatoid factor-negative polyarticular juvenile idiopathic arthritisHP:0040283 - Occasional
HP:0001530HP:0001530Mild postnatal growth retardation0PTPN22 CL E G H261919652ORPHA:85408Rheumatoid factor-negative polyarticular juvenile idiopathic arthritisHP:0040283 - Occasional3
HP:0001530HP:0001530Mild postnatal growth retardation0PTRH2 CL E G H5165124265ORPHA:456312Infantile multisystem neurologic-endocrine-pancreatic diseaseHP:0040282 - Frequent6
HP:0001530HP:0001530Mild postnatal growth retardation0STAT4 CL E G H677511365ORPHA:85408Rheumatoid factor-negative polyarticular juvenile idiopathic arthritisHP:0040283 - Occasional2


Genes (16) :ADAMTS3 ANKRD55 CCBE1 CD247 CDAN1 ERCC6 ERCC8 FAT4 IGFALS IL2RA IL2RB PRKAR1A PTPN2 PTPN22 PTRH2 STAT4

Diseases (8) :ORPHA:2136 ORPHA:85408 OMIM:235510 OMIM:224120 ORPHA:90324 OMIM:615961 OMIM:101800 ORPHA:456312
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.