Human Phenotype Ontology 
Grandparent Node:
All (HP:0000001)help
Parent Node:
Mode of inheritance (HP:0000005)help
..Starting node
obsolete Gonosomal inheritance (HP:0010985)help
Term ID: 10985
Name: obsolete Gonosomal inheritance
Reference: HP:0010985
Genes and Diseases:
       Child Nodes:
........expandX-linked inheritance (HP:0001417) help
................... HP:0001419 X-linked recessive inheritance
................... HP:0001423 X-linked dominant inheritance
........expandY-linked inheritance (HP:0001450) help

 Sister Nodes: 
..expandAutosomal dominant inheritance (HP:0000006) help
..expandAutosomal recessive inheritance (HP:0000007) help
..expandContiguous gene syndrome (HP:0001466) help
..expandGenetic anticipation (HP:0003743) help
..expandMitochondrial inheritance (HP:0001427) help
..expandMultifactorial inheritance (HP:0001426) help
..expandobsolete Familial predisposition (HP:0001472) help
..expandobsolete Heterogeneous (HP:0001425) help
..expandSomatic mutation (HP:0001428) help
..expandSporadic (HP:0003745) 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:0010985HP:0010985obsolete Gonosomal inheritance0 CL E G H

Genes (0) :

Diseases (0) :

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