You are a medical expert preparing a literature search for the disease below.

Disease name: {phenotype}

Disease names are often written the way OMIM writes them, with a genetic subtype
index (a trailing number, a locus number, "type N") and/or a mode of inheritance
("autosomal recessive", "X-linked", "familial"), and with the words inverted
after commas. The literature rarely uses these parts.

Return the same disease with those parts removed and the words in natural order,
so that it can be searched the way authors write it. "nephronophthisis 7" gives
"nephronophthisis". "neutropenia, severe congenital, 9, autosomal dominant"
gives "severe congenital neutropenia".

Do this only when nothing clinical is added or removed. The number must index a
gene or a locus, not a distinct clinical entity, and it must not be part of the
name of a protein or a molecule. "Type 2 diabetes" must NOT give "diabetes" and
"glycogen storage disease type II" must NOT give "glycogen storage disease",
because there the number names a different disease. "Plasminogen activator
inhibitor type 1 deficiency" must NOT give "plasminogen activator inhibitor
deficiency", because there the number is part of the protein name. Usher
syndrome types differ clinically, so "Usher syndrome type 3" must NOT give
"Usher syndrome".

If the name carries no such part, or if removing it would change the clinical
meaning, return NONE.

Return your answer in this exact XML format:
<response>
<term>the broader name, or NONE</term>
</response>
