46,XX testicular disorder of sex development
|
(Orphanet:393)
|
46,XY SEX REVERSAL 7
|
(OMIM:233420)
|
46,XY complete gonadal dysgenesis
|
(Orphanet:242)
|
Autosomal dominant popliteal pterygium syndrome
|
(Orphanet:1300)
|
CHONDRODYSPLASIA, ACROMESOMELIC, WITH GENITAL ANOMALIES
|
(OMIM:609441)
|
Classic Mayer-Rokitansky-Küster-Hauser syndrome
|
(Orphanet:247775)
|
Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency
|
(Orphanet:90795)
|
HYPOGONADOTROPIC HYPOGONADISM 13 WITH OR WITHOUT ANOSMIA
|
(OMIM:614842)
|
HYPOGONADOTROPIC HYPOGONADISM 8 WITH OR WITHOUT ANOSMIA
|
(OMIM:614837)
|
Insulin-resistance syndrome type A
|
(Orphanet:2297)
|
MICROPHTHALMIA, SYNDROMIC 7
|
(OMIM:309801)
|
MURCS association
|
(Orphanet:2578)
|
Matthew-Wood syndrome
|
(Orphanet:2470)
|
Mulibrey nanism
|
(Orphanet:2576)
|
Perrault Syndrome 1
|
(OMIM:233400)
|
Perrault Syndrome 3
|
(OMIM:614129)
|
Perrault Syndrome 4
|
(OMIM:615300)
|
Peters-plus syndrome
|
(Orphanet:709)
|
Renal cysts and diabetes syndrome
|
(Orphanet:93111)
|
SATOYOSHI SYNDROME
|
(OMIM:600705)
|
Woodhouse-Sakati syndrome
|
(Orphanet:3464)
|