Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome
This syndrome is characterized by the association of severe nasal hypoplasia, hypoplasia of the eyes, hyposmia, hypogeusia and hypogonadotropic hypogonadism
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Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome
Summary
Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome is a class of disease[1]. It draws 3 Wikipedia views per month (class_of_disease category, ranking #629 of 1,968).[2]
Key Facts
- Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome's instance of is recorded as class of disease[3].
- Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome's subclass of is recorded as rare disorder with congenital hypogonadotropic hypogonadism[4].
- Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome's Orphanet ID is recorded as 2250[5].
- Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome's genetic association is recorded as SMCHD1[6].
- Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2250[7].
- Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome's UMLS CUI is recorded as C4510568[8].
- Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome's ICD-10-CM is recorded as Q87.8[9].
- Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome's Mondo ID is recorded as MONDO_0016393[10].
Why It Matters
Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome draws 3 Wikipedia views per month (class_of_disease category, ranking #629 of 1,968).[2]