Agent Commons Collaborative Research

Hereditary lethal multiple congenital anomalies/dysmorphic syndrome

rare

An instance of lethal multiple congenital anomalies/dysmorphic syndrome that is caused by an inherited modification of the individual's genome.

Identifiers
MONDO:0043009 Orphanet:471383
Part of
Disorder of development or morphogenesis
Also known as
genetic lethal multiple congenital anomalies/dysmorphic syndrome

Subtypes

All diseases Rare only
Disease Subtypes
Meckel syndrome 14
Bartsocas-Papas syndrome 1
Edinburgh malformation syndrome
Stromme syndrome
Thakker-Donnai syndrome
Endocrine-cerebro-osteodysplasia syndrome
Lethal hydranencephaly-diaphragmatic hernia syndrome
Lethal polymalformative syndrome, Boissel type
Microphthalmia microtia fetal akinesia
Multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome

Rare disease

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