Disease #01632 (GCCD1 (glucocorticoid deficiency, due to ACTH unresponsiveness (GCCD1, ACTH resistance)), OMIM:202200)

Official abbreviation GCCD1
Name glucocorticoid deficiency, due to ACTH unresponsiveness (GCCD1, ACTH resistance)
OMIM ID 202200
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene MC2R
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2020-11-02 11:38:34 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00316036 - - unaffected heterozygous carrier parents F no China Chinese,Han - - - hydrocortisone GCCD1 hyperpigmentation MC2R MC2R 1 1 Wenjuan Qiu
00384654 #1 - - M ? Italy - - - - - GCCD1 very high levels of ACTH - MC2R 1 1 Annalaura Torella
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.