[[File:H syndrome.jpg|thumb|The H syndrome flag.]]
'''H Syndrome''', '''Histiocytosis-lymphadenopathy plus syndrome''', or '''PHID''', is a conditionsyndrome that may or may not be considered an [[intersex]] conditionvariation, or it may be considered a conditionsyndrome that comes with intersex traits, depending on who you ask.
Those with this conditionsyndrome tend to have [[hypogonadism]], darker skin than usual for their race (hyperpigmentation), more hair growth than usual (hypertrichosis), hearing loss, heart anomalies, low height, hyperglycemia, hallux valgus, and hepatosplenomegaly (enlarged spleen and liver).
It is important to note that not all the symptoms listed in this page are guaranteed to occur in someone with this conditionsyndrome, as someone may only experience one or several of these symptoms, yet still hold the conditionsyndrome.
== Causes ==
This conditionsyndrome is caused by a mutation within the ''SLC29A3'' gene, which is a gene that helps encode important proteins within the human body.
== History ==
This conditionsyndrome was first described in 1998.
== Flag ==
== Etymology ==
This conditionsyndrome was named "H Syndrome" due to most of the symptoms starting with the letter H.
== Resources ==
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