ORPHA:370006

Hypothalamic insufficiency-secondary microcephaly-visual impairment-urinary anomalies syndrome

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Septo-optic dysplasia spectrum

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Hypothalamic insufficiency-secondary microcephaly-visual impairment-urinary anomalies syndrome
fr	Syndrome d'insuffisance hypophysaire multiple-microcéphalie secondaire-cécité-anomalies urinaires
de	Hypothalamusinsuffizienz-sekundäre Mikrozephalie-Sehschwäche-Harnwegsanomalien-Syndrom
es	Síndrome de insuficiencia hipotalámica-microcefalia secundaria-discapacidad visual-anomalías urinarias
it	Sindrome insufficienza ipotalamica-microcefalia secondaria-difetto visivo-anomalie urinarie
nl	Hypothalamusinsufficiëntie - secundaire microcefalie - visuele beperking - urineweganomalieën-syndroom
pt	Síndrome de insuficiência hipotalâmica-microcefalia secundária-défice visual-anomalias urinárias
pl	Niedoczynność podwzgórza-wtórne małogłowie-upośledzenie wzroku-wady układu moczowego
cs	Syndrom zahrnující hypotalamickou nedostatečnost, sekundární mikrocefalii, postižení zraku a anomálie močového traktu
uk	Синдром гіпоталамічної недостатності-вторинної мікроцефалії-порушення зору-аномалій сечовивідної системи
zh	下丘脑功能不全-继发性小头畸形-视觉损害-尿路异常综合征
tr	Hipotalamik yetmezlik-sekonder mikrosefali-görme bozukluğu-üriner anomaliler sendromu

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
OMIM	615926	E		validated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

Not placed in any Orphanet classification in this release.

No children.

0 direct

Orphanet records no gene directly on this code.

0 records

No prevalence record in this release.

Orphanet has no HPO annotation for this code in this release.