Human Phenotype Ontology 
..Starting node
..expandDelayed ability to roll over (HP:0032989)help
Term ID: 32989
Name: Delayed ability to roll over
Synonym:
Definition: Delayed ahcievement of the ability to roll front to back and back to front.
Comments:
Reference: HP:0032989
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0032989HP:0032989Delayed ability to roll over0ADCY5 CL E G H111236OMIM:619651NEURODEVELOPMENTAL DISORDER WITH HYPERKINETIC MOVEMENTS AND DYSKINESIA; NEDHYD25
HP:0032989HP:0032989Delayed ability to roll over0ATP6V0A1 CL E G H535865OMIM:6199701
HP:0032989HP:0032989Delayed ability to roll over0CELF2 CL E G H106592550OMIM:619561DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 97; DEE97
HP:0032989HP:0032989Delayed ability to roll over0MECP2 CL E G H42046990OMIM:300260Mental retardation, x-linked syndromic, Lubs type950
HP:0032989HP:0032989Delayed ability to roll over0MRPS25 CL E G H6443214511OMIM:619025COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 50; COXPD50
HP:0032989HP:0032989Delayed ability to roll over0NDUFA8 CL E G H47027692OMIM:619272MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 37; MC1DN37
HP:0032989HP:0032989Delayed ability to roll over0PGAP1 CL E G H8005525712OMIM:615802MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42; MRT4220
HP:0032989HP:0032989Delayed ability to roll over0SLC25A12 CL E G H860410982OMIM:612949Epileptic encephalopathy, early infantile, 3944
HP:0032989HP:0032989Delayed ability to roll over0SON CL E G H665111183OMIM:617140Zttk syndrome12
HP:0032989HP:0032989Delayed ability to roll over0TAF8 CL E G H12968517300OMIM:619972
HP:0032989HP:0032989Delayed ability to roll over0VPS35L CL E G H5702024641OMIM:619135RITSCHER-SCHINZEL SYNDROME 3; RTSC3
HP:0032989HP:0032989Delayed ability to roll over0YIF1B CL E G H9052230511OMIM:619125KAYA-BARAKAT-MASSON SYNDROME; KABAMAS


Genes (12) :ADCY5 ATP6V0A1 CELF2 MECP2 MRPS25 NDUFA8 PGAP1 SLC25A12 SON TAF8 VPS35L YIF1B

Diseases (12) :OMIM:619651 OMIM:619970 OMIM:619561 OMIM:300260 OMIM:619025 OMIM:619272 OMIM:615802 OMIM:612949 OMIM:617140 OMIM:619972 OMIM:619135 OMIM:619125
 

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