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Phenotypic Abnormality (PA): Abnormality of the menstrual cycle

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Root: HP Hierarchy (human phenotype with 3 sub-ontologies PA, MI, ON)

Shortest distance to current term (+ for parents, - for children) HP term [HP ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + + + 5:   Abnormality of the genitourinary system [HP:0000119] <5>(74|72) (79|29|9)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the genital system [HP:0000078] <3>(34|34) (36|10|3)
+ + + 3:   Abnormality of the endocrine system [HP:0000818] <16>(30|34) (35|12|5)
+ + + 3:   Abnormal reproductive system morphology [HP:0012243] <10>(27|26) (27|4|1)
+ + 2:   Abnormality of the female genitalia [HP:0010460] <2>(16|18) (18|2|0)
+ + 2:   Puberty and gonadal disorders [HP:0008373] <13>(17|18) (20|3|1)
+ + 2:   Abnormal internal genitalia [HP:0000812] <9>(15|17) (16|2|0)
+ 1:   Abnormality of female internal genitalia [HP:0000008] <5>(14|16) (16|2|0)
+ 1:   Menstrual irregularities [HP:0000858] <2>(6|8) (7|0|0)
0:   Abnormality of the menstrual cycle [HP:0000140] <7>(6|8) (7|0|0)
- 1:   Amenorrhea [HP:0000141] <2>(3|4) (4|0|0)
- 1:   Delayed menarche [HP:0012569](0|0) (0|0|0)
- 1:   Menometrorrhagia [HP:0400008](2|2) (2|0|0)
- 1:   Menorrhagia [HP:0000132](1|2) (1|0|0)
- 1:   Metrorrhagia [HP:0100608](0|0) (0|0|0)
- 1:   Oligomenorrhea [HP:0000876](0|0) (0|0|0)
- 1:   Polymenorrhea [HP:0400007](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Smc hinge domain0Direct
Fibrinogen coiled-coil and central regions0Direct
NagB/RpiA/CoA transferase-like0.0002057Direct
Nuclear receptor ligand-binding domain0.02919Inherited
Trypsin-like serine proteases0.07175Inherited
Fibrinogen C-terminal domain-like0.1293Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Smc hinge domain0Direct
IF2B-like0Direct
Fibrinogen coiled-coil and central regions0Direct
Ngr ectodomain-like0.008445Inherited
Nuclear receptor ligand-binding domain0.02618Inherited
Eukaryotic proteases0.0406Inherited
Nuclear receptor0.04313Inherited
Fibrinogen C-terminal domain-like0.1171Inherited


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
Smc hinge domain0Direct
Fibrinogen coiled-coil and central regions0Direct
NagB/RpiA/CoA transferase-like0.0001023Direct
Nuclear receptor ligand-binding domain0.02058Inherited
Trypsin-like serine proteases0.05505Inherited
Glucocorticoid receptor-like (DNA-binding domain)0.06244Inherited
Fibrinogen C-terminal domain-like0.1045Inherited


Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
Plot tree as:   Download Newick format tree:
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