occipital horn syndrome
Occipital horn syndrome (OHS) is a mild form of Menkes disease (MD, see this term), a syndrome characterized by progressive neurodegeneration and connective tissue disorders due to a copper transport defect
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occipital horn syndrome
Summary
occipital horn syndrome is a developmental defect during embryogenesis[1]. It draws 42 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #126 of 308).[2]
Key Facts
- occipital horn syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- occipital horn syndrome's instance of is recorded as designated intractable/rare disease[4].
- occipital horn syndrome's instance of is recorded as rare disease[5].
- occipital horn syndrome's instance of is recorded as class of disease[6].
- occipital horn syndrome is a type of copper metabolism disease[7].
- occipital horn syndrome is a type of multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome[8].
- occipital horn syndrome is a type of developmental anomaly of metabolic origin[9].
- occipital horn syndrome's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4555[10].
- occipital horn syndrome's health specialty is recorded as endocrinology[11].
- occipital horn syndrome's genetic association is recorded as ATP7A[12].
- occipital horn syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_198[13].
- occipital horn syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111272[14].
- occipital horn syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
Why It Matters
occipital horn syndrome draws 42 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #126 of 308).[2]