hereditary lethal multiple congenital anomalies/dysmorphic syndrome
MONDO:0043009Mondo
Findings
No curated finding names hereditary lethal multiple congenital anomalies/dysmorphic syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
An instance of lethal multiple congenital anomalies/dysmorphic syndrome that is caused by an inherited modification of the individual's genome.
Definition from the Mondo Disease Ontology (MONDO:0043009), read 2026-09-29. CC BY 4.0.
Where it sits
- Narrower terms (10)
- Bartsocas-Papas syndrome 1
- Edinburgh malformation syndrome
- endocrine-cerebro-osteodysplasia syndrome
- lethal hydranencephaly-diaphragmatic hernia syndrome
- lethal polymalformative syndrome, Boissel type
- Meckel syndrome
- microphthalmia microtia fetal akinesia
- multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome
- Stromme syndrome
- Thakker-Donnai syndrome
Other names
1 name
Resolves to: hereditary lethal multiple congenital anomalies/dysmorphic syndrome
- Also called
- genetic lethal multiple congenital anomalies/dysmorphic syndrome