Disorder of reproductive system
Hereditary disorder by system
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Reproductive system hereditary disorder (disorder)
Reproductive system hereditary disorder
hereditaire aandoening van voortplantingsstelsel
erfelijke ziekte van voortplantingssysteem
Id363290007
StatusDefined
Finding siteStructure of anatomical reproductive system
ICD-10 complex map reference set
Target
RuleTRUE
AdviceMAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA
CorrelationSNOMED CT source code to target map code correlation not specified
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3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency
46,XX disorder of sex development with skeletal anomalies syndrome
46,XY disorder of sex development due to isolated 17,20-lyase deficiency
46,XY disorder of sex development, adrenal insufficiency due to CYP11A1 deficiency
46,XY gonadal dysgenesis, motor and sensory neuropathy syndrome
46,XY partial gonadal dysgenesis
4H leukodystrophy3
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome
Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome
Alopecia, progressive neurological defect, endocrinopathy syndrome
Boucher Neuhäuser syndrome
Chondrodysplasia with disorder of sex development syndrome
Colobomatous microphthalmia, obesity, hypogenitalism, intellectual disability syndrome
Congenital cataract with deafness and hypogonadism syndrome
Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome
Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome
Deafness and hypogonadism syndrome
Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome
Dysmorphism, short stature, deafness, disorder of sex development syndrome
Familial adrenal hypoplasia with absent pituitary luteinizing hormone
Familial male-limited precocious puberty
Familial penile hypospadias
Female infertility due to oocyte meiotic arrest
Female infertility due to zona pellucida defect
Frontonasal dysplasia with alopecia and genital anomaly syndrome
Genitopalatocardiac syndrome
Haspeslagh Fryns Muelenaere syndrome
Hereditary breast and ovarian cancer syndrome
Hereditary endometrial carcinoma
Hereditary malignant epithelial tumor of ovary
Hereditary site-specific ovarian cancer syndrome
Hydrocephalus with obesity and hypogonadism syndrome
Hydrocephalus with obesity and hypogonadism syndrome
Hyperandrogenism due to cortisone reductase deficiency
Hypergonadotropic hypogonadism with cataract syndrome
Hypergonadotropic hypogonadism with cataract syndrome
Hypogonadism with prune belly syndrome
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome
Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome
Hypogonadotropic hypogonadism, severe microcephaly, sensorineural hearing loss, dysmorphism syndrome
Intellectual disability, myopathy, short stature, endocrine defect syndrome
Kallman syndrome with heart disease
Leydig cell agenesis3
Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome
MacDermot Winter syndrome
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome
Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome
McKusick Kaufman syndrome
Microcephalic primordial dwarfism, insulin resistance syndrome
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome
MIRAGE syndrome
MORM syndrome
Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome
Obesity due to leptin receptor gene deficiency
Opitz-Frias syndrome
Ovarioleukodystrophy
Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome
Partial androgen insensitivity syndrome1
Primary hypergonadotropic hypogonadism and partial alopecia syndrome
Progressive cerebellar ataxia with hypogonadism
RAB18 deficiency2
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome
SCARF syndrome
Scholte syndrome
Sclerosing dysplasia of bone, ichthyosis, premature ovarian failure syndrome
Sclerosing dysplasia of bone, ichthyosis, premature ovarian failure syndrome
Sensorineural deafness and male infertility
SERKAL syndrome
Spastic paraplegia with precocious puberty syndrome
Splenogonadal fusion, limb defect, micrognathia syndrome
Syndromic X-linked intellectual disability type 7
Urban Rogers Meyer syndrome
WNT4 Mullerian aplasia and ovarian dysfunction
Woodhouse Sakati syndrome
X-linked central congenital hypothyroidism with late-onset testicular enlargement
X-linked intellectual disability Cilliers type
X-linked intellectual disability Van Esch type
X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome
X-linked lissencephaly with abnormal genitalia syndrome
XY type gonadal dysgenesis with associated anomalies syndrome