Disease #00562 (HRDS (Hypoparathyroidism-retardation-dysmorphism syndrome), OMIM:241410)

Official abbreviation HRDS
Name Hypoparathyroidism-retardation-dysmorphism syndrome
OMIM ID 241410
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene TBCE
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

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