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Phenotypic Abnormality (PA): Abnormality of the nail

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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)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + 2:   Abnormality of the integument [HP:0001574] <4>(48|69) (59|37|15)
+ 1:   Abnormality of skin adnexa morphology [HP:0011138] <5>(16|19) (17|6|2)
0:   Abnormality of the nail [HP:0001597] <25>(5|5) (5|3|1)
- 1:   Nail dysplasia [HP:0002164] <15>(0|0) (0|0|0)
- 1:   Abnormal toenail morphology [HP:0008388] <8>(2|2) (2|0|0)
- 1:   Abnormal fingernail morphology [HP:0001231] <6>(2|2) (2|0|0)
- 1:   Aplasia/Hypoplasia of the nails [HP:0008386] <4>(2|3) (2|0|0)
- 1:   Abnormality of nail color [HP:0100643] <3>(0|0) (0|0|0)
- 1:   Abnormality of the periungual region [HP:0100803] <3>(1|1) (1|1|1)
- 1:   Abnormality of the subungual region [HP:0009723] <3>(0|0) (0|0|0)
- 1:   Nail dystrophy [HP:0008404] <3>(2|2) (2|2|0)
- 1:   Onychogryposis [HP:0001805] <3>(1|1) (1|1|0)
- 1:   Onycholysis [HP:0001806] <3>(0|1) (0|0|1)
- 1:   Abnormal nail growth [HP:0030807] <2>(0|0) (0|0|0)
- 1:   Thin nail [HP:0001816] <2>(0|0) (0|0|0)
- 1:   Neoplasm of the nail [HP:0100826] <1>(0|0) (0|0|0)
- 1:   Absent lunula [HP:0030805](0|0) (0|0|0)
- 1:   Beaked nails [HP:0030817](0|0) (0|0|0)
- 1:   Chronic monilial nail infection [HP:0008396](0|0) (0|0|0)
- 1:   Fragile nails [HP:0001808](0|1) (0|0|0)
- 1:   Ingrown nail [HP:0012710](0|0) (0|0|0)
- 1:   Nail bed hemorrhage [HP:0030254](0|0) (0|0|0)
- 1:   Nail bed telangiectasia [HP:0001232](0|0) (0|0|0)
- 1:   Pterygium of nails [HP:0002165](0|0) (0|0|0)
- 1:   Pyramidal skinfold extending from the base to the top of the nails [HP:0009758](0|0) (0|0|0)
- 1:   Ragged cuticle [HP:0030808](0|0) (0|0|0)
- 1:   Recurrent loss of toenails and fingernails [HP:0008390](0|0) (0|0|0)
- 1:   Ski jump nail [HP:0030819](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Plakin repeat0Direct
Intermediate filament protein, coiled coil region0.001012Inherited
ARID-like0.07262Inherited
HMG-box0.1638Inherited
EGF/Laminin0.4035Inherited


Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Plakin repeat0Direct
Intermediate filament protein, coiled coil region0.0008026Direct
ARID domain0.06212Inherited
Laminin-type module0.1498Inherited
HMG-box0.1515Inherited


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)
Plakin repeat0Direct
Intermediate filament protein, coiled coil region0.0005384Direct
ARID-like0.05551Inherited
HMG-box0.1343Inherited
EGF/Laminin0.3602Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
75399,75399
  • 75399 - Plakin repeat
  • 75399 - Plakin repeat
  • 0Direct
    64593,64593
  • 64593 - Intermediate filament protein, coiled coil region
  • 64593 - Intermediate filament protein, coiled coil region
  • 0.01205Inherited
    57196,57196
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 0.1667Inherited

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    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    57196,57196,57196
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 0.03715Inherited


    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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