Occipital horn syndrome
MONDO:0010572Occipital horn syndrome (OHS) is a mild form of Menkes disease (MD), a syndrome characterized by progressive neurodegeneration and connective tissue disorders due to a copper transport defect.
Also known as: occipital horn syndrome, occipital horn syndrome, X-linked recessive, EDS IX (formerly), EDS IX, formerly, EDS9, EDS9, formerly, Ehlers-Danlos syndrome, occipital horn type, Ehlers-Danlos syndrome, occipital horn type (formerly)
1 clinical trial for this condition and its sub-types.
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Disease
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Metabolic disease
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Hereditary disease
(176)
Inborn errors of metabolism
(45)
Cutis laxa
(37)
Human disease
(14)
Developmental defect during embryogenesis
(8)
Disease of genetic or genomic mechanism
(2)
Multiple congenital anomalies/dysmorphic syndrome
(1)
Developmental anomaly of metabolic origin
(0)