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Phenotypes for disease #03221 (SRXY3 (46,XY sex reversal, type 3 (SRXY-3)), OMIM:612965)
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Please note that a short description of a certain column can be displayed when you move your mouse cursor over the column's header and hold it still. Below, a more detailed description is shown per column.
Phenotype details
: additional information on the phenotype of the individual, preferably use HPO terms only (http://www.human-phenotype-ontology.org/)
Diagnosis/Initial
: initial diagnosis, before molecular testing
Diagnosis/Definite
: phenotype individual after molecular testing (OMIM abbreviation)
Inheritance
: Indicates the inheritance of the phenotype in the family; unknown, familial (autosomal/X-linked, dominant/ recessive), paternal (Y-linked), maternal (mitochondrial), isolated (sporadic) or complex
All options:
Unknown
Familial
Familial, autosomal dominant
Familial, autosomal recessive
Familial, X-linked
Familial, X-linked dominant
Familial, X-linked dominant, male sparing
Familial, X-linked recessive
Paternal, Y-linked
Maternal, mitochondrial
Isolated (sporadic)
Di-genic
Complex
- = Not applicable
Age/Examination
: age at which the individual was examined.
35y = 35 years
04y08m = 4 years and 8 months
00y00m01d12h = 1 day and 12 hours
18y? = around 18 years
30y-40y = between 30 and 40 years
>54y = older than 54
? = unknown
Age/Diagnosis
: age diagnosis was confirmed
35y = 35 years
04y08m = 4 years and 8 months
00y00m01d12h = 1 day and 12 hours
18y? = around 18 years
30y-40y = between 30 and 40 years
>54y = older than 54
? = unknown
Age/Onset
: Age first symptoms disease appeared in individual:
35y = 35 years
04y08m = 4 years and 8 months
00y00m01d12h = 1 day and 12 hours
18y? = around 18 years
30y-40y = between 30 and 40 years
>54y = older than 54
? = unknown
Phenotype/Onset
: individual's phenotype at Age/Onset described using HPO
Protein
: result from protein staining
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Date
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Date
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Date
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Date
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Numeric
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Numeric
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Numeric
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Numeric
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all entries containing 'South Asian', but not containing 'South East Asian'
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16 entries on 1 page. Showing entries 1 - 16.
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How to query
Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000171793
urethral opening penoscrotal, gonadal location (L/R) labioscrotal folds, low basal testosterone, partial testosterone response to hCG testing, dysgenetic testes bilaterally
46,XY DSD
-
Unknown
-
-
00y04m
-
-
Helena Fabbri-Scallet
00226682
0000171794
1.5 cm phallus, both gonads palpable in the inguinal channel, no Müllerian derivatives.
-
-
Unknown
-
-
-
-
-
Helena Fabbri-Scallet
00227771
0000171795
5.5 cm phallus with chordee, penoscrotal urethral opening, right gonad palpable in inguinal channel and left gonad palpable in labioscrotal fold. No Müllerian derivatives.
-
46,XY partial gonadal dysgenesis
Unknown
-
-
-
-
-
Helena Fabbri-Scallet
00227772
0000171796
3.5 cm phallus with chordee, perineal urethral opening and both gonads palpable in labioscrotal folds. Male internal genitalia, with no uterus. Dysgenetic testis bilaterally.
-
46,XY partial gonadal dysgenesis
Unknown
-
-
-
-
-
Helena Fabbri-Scallet
00227773
0000171797
2-cm phallus, single perineal opening, palpable gonads in the labioscrotal folds. Laboratory data indicated high levels of FSH but normal levels of LH, and a normal testosterone response to hCG test. Absence of mullerian derivatives.
-
-
Unknown
-
-
-
-
-
Helena Fabbri-Scallet
00227774
0000171840
2.5 cm phallus with chordee, single penoscrotal urethral opening, bilaterally palpable gonads in the inguinal region. Streak gonad showing fibrous tissue without gonadal elements only on the right side and a dysgenetic testis on the left side.
-
46,XY partial gonadal dysgenesis
Unknown
-
-
-
-
-
Helena Fabbri-Scallet
00227818
0000171863
2.3 cm phallus with chordee and 2 urethral orifices, both gonads palpable on inguinal channel, no Müllerian derivatives. Dysgenetic testis.
-
46,XY partial gonadal dysgenesis
Unknown
-
-
-
-
-
Helena Fabbri-Scallet
00227861
0000171864
1 cm phallus with chordee and a penoscrotal urethral opening, gonads were not palpable, no Müllerian derivatives. Dysgenetic testis.
-
46,XY partial gonadal dysgenesis
Unknown
-
-
-
-
-
Helena Fabbri-Scallet
00227862
0000171865
see paper; ..., normal adrenal phenotype, male external genitalia, absent Müllerian cells, normal testis
mild oligozoospermia
-
Unknown
-
-
-
-
-
Johan den Dunnen
00165039
0000171866
see paper; ..., complete gonadal dysgenesis, female external genitalia, normal adrenal phenotype, Müllerian cells present, streak gonads (no evidence of tubules)
severe 46,XY sex reversal, complete gonadal dysgenesis
SRXY-3
Unknown
16y
-
-
-
-
Johan den Dunnen
00165040
0000173066
Urethral penoscrotal opening, palpable gonads in the labioscrotal folds. Absence of mullerian derivatives.
-
46,XY partial gonadal dysgenesis
Unknown
-
-
-
-
-
Helena Fabbri-Scallet
00230585
0000173067
Perineal urethral opening, predominantly female external genitalia, no palpable gonads. Presence of uterus. Dysgenetic testis.
-
46,XY partial gonadal dysgenesis
Unknown
-
-
-
-
-
Helena Fabbri-Scallet
00230586
0000173068
single penoscrotal urethral opening, palpable gonads, normal testosterone production
-
-
Unknown
-
-
-
-
-
Helena Fabbri-Scallet
00230587
0000173069
Primary amenorrhea and absence of secondary female sex characteristics. 3-cm phallus, female urethra and a vaginal opening, no gonads were palpable. Mullerian derivatives absent. Dysgenetic testis.
-
46,XY partial gonadal dysgenesis
Unknown
-
-
-
-
-
Helena Fabbri-Scallet
00230588
0000173070
single perineal opening, palpable gonads in the labioscrotal folds. Absence of mullerian derivatives. Dysgenetic testis.
-
46,XY partial gonadal dysgenesis
Unknown
-
-
-
-
-
Helena Fabbri-Scallet
00230589
0000186688
urethral opening penoscrotal, gonadal location (L/R) in labioscrotal folds, dysgenetic testes bilaterally
-
Partial GD
Unknown
-
-
-
-
-
Helena Fabbri-Scallet
00246900
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