MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
  Most Studied  CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO
Disease Browser
Parent Node:
expandendocrine system disease (MONDO:0005151)
..Starting node
..expandgenetic endocrine growth disease ()

       Child Nodes:
........expandcataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome ()
........expandcongenital adrenal hyperplasia ()
........expandgrowth hormone insensitivity syndrome ()
........expandinherited primary ovarian failure ()
........expandmicrodontia hypodontia short stature ()
........expandnon-acquired pituitary hormone deficiency ()
........expandpermanent congenital hypothyroidism ()
........expandzerres rietschel majewski syndrome ()



 Sister Nodes: 
..expandadrenal gland disease ()
..expandautoimmune disease of endocrine system ()
..expandcholedocholithiasis ()
..expandendocrine gland neoplasm ()
..expandendocrine tuberculosis ()
..expandestrogen resistance syndrome ()
..expandgenetic endocrine growth disease ()
..expandgonadal disease ()
..expandhyperinsulinemic hypoglycaemia ()
..expandhypoinsulinemic hypoglycemia and body hemihypertrophy ()
..expandliver disease ()
..expandmonogenic obesity ()  LSDB  L: 00114;
..expandneuroendocrine disease ()
..expandnon-neoplastic bile duct disorder ()
..expandpancreas disease ()
..expandparathyroid gland disease ()
..expandpolycystic ovary syndrome ()
..expandpolyendocrinopathy ()
..expandrare endocrine growth disease ()
..expandrare genetic hypothalamic or pituitary disease ()
..expandrare hypothalamic or pituitary disease ()
..expandrare parathyroid disease and phosphocalcic metabolism anomaly ()
..expandthymus gland disease ()
..expandthyroid gland disease ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:15514
Name:genetic endocrine growth disease
Definition:
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:growth disorder
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal