Human Phenotype Ontology 
Grandparent Node:
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Diabetes mellitus (HP:0000819)help
Grandparent Node:
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Insulin resistance (HP:0000855)help
Parent Node:
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Insulin-resistant diabetes mellitus (HP:0000831)help
..Starting node
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Insulin-resistant diabetes mellitus at puberty (HP:0000877)help
Term ID: 877
Name: Insulin-resistant diabetes mellitus at puberty
Synonym: Insulin-resistant diabetes mellitus at puberty
Definition:
Comments:
Reference: HP:0000877
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandNeonatal insulin-dependent diabetes mellitus (HP:0000857) 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:0000877HP:0000877Insulin-resistant diabetes mellitus at puberty0AGPAT2 CL E G H10555325OMIM:608594Lipodystrophy, congenital generalized, type 1.85
HP:0000877HP:0000877Insulin-resistant diabetes mellitus at puberty0BSCL2 CL E G H2658015832OMIM:269700Lipodystrophy, congenital generalized, type 2.105
HP:0000877HP:0000877Insulin-resistant diabetes mellitus at puberty0PLIN1 CL E G H53469076ORPHA:280356PLIN1-related familial partial lipodystrophyHP:0040280 - Obligate19


Genes (3) :AGPAT2 BSCL2 PLIN1

Diseases (3) :OMIM:608594 OMIM:269700 ORPHA:280356
 

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