Hallermann-Streiff syndrome
congenital disorder
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Hallermann-Streiff syndrome
Summary
Hallermann-Streiff syndrome is a developmental defect during embryogenesis[1]. It draws 278 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #67 of 308).[2]
Key Facts
- Hallermann-Streiff syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Hallermann-Streiff syndrome's instance of is recorded as class of disease[4].
- Hallermann-Streiff syndrome is a type of syndrome[5].
- Hallermann-Streiff syndrome is a type of Slender bone dysplasia[6].
- Hallermann-Streiff syndrome is a type of congenital absence of the eyebrow/eyelashes[7].
- Hallermann-Streiff syndrome is a type of ectodermal malformation syndrome associated with ocular features[8].
- Hallermann-Streiff syndrome is a type of craniofacial anomaly with cataract[9].
- Hallermann-Streiff syndrome is a type of multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome[10].
- Hallermann-Streiff syndrome is a type of malformation syndrome with short stature[11].
- Hallermann-Streiff syndrome is a type of genetic syndromic intellectual disability[12].
- Hallermann-Streiff syndrome's Commons category is recorded as Hallermann-Streiff syndrome[13].
- Hallermann-Streiff syndrome's NCI Thesaurus ID is recorded as C84746[14].
- Hallermann-Streiff syndrome's health specialty is recorded as medical genetics[15].
- Hallermann-Streiff syndrome's genetic association is recorded as GJA1[16].
- Hallermann-Streiff syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_4534[17].
- Hallermann-Streiff syndrome's exact match is recorded as http://identifiers.org/doid/DOID:4534[18].
- Hallermann-Streiff syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2108[19].
- Hallermann-Streiff syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[20].
Why It Matters
Hallermann-Streiff syndrome draws 278 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #67 of 308).[2] It has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[21] It is known by 21 alternative names across languages and contexts.[22]