General Information of Disease (ID: DISOGTFT)

Disease Name Hereditary lethal multiple congenital anomalies/dysmorphic syndrome
Synonyms genetic lethal multiple congenital anomalies/dysmorphic syndrome
Definition An instance of lethal multiple congenital anomalies/dysmorphic syndrome that is caused by an inherited modification of the individual's genome.
Disease Hierarchy
DISQCXZX: Disorder of development or morphogenesis
DISOGTFT: Hereditary lethal multiple congenital anomalies/dysmorphic syndrome
Disease Identifiers
MONDO ID
MONDO_0043009
UMLS CUI
C5681265
MedGen ID
1843298
Orphanet ID
471383