Disease #00654 (HH5 (hypogonadism, hypogonadotropic, type 5 with/without anosmia (HH-5)), OMIM:612370)

Official abbreviation HH5
Name hypogonadism, hypogonadotropic, type 5 with/without anosmia (HH-5)
OMIM ID 612370
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene CHD7
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00430229 20D2602992 - - M no China East Asia - - - - HH5 Micropenis; cleft lip/palate; hearing loss; testicular hypotrophy; aplasia of bilateral olfactory-bulb CHD7 CHD7 1 1 Dongye He
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