Human Phenotype Ontology 
Grandparent Node:
Abnormality of skin morphology (HP:0011121)help
Parent Node:
Localized skin lesion (HP:0011355)help
..Starting node
Molluscoid pseudotumors (HP:0000993)help
Term ID: 993
Name: Molluscoid pseudotumors
Synonym: Molluscoid pseudotumor
Definition: Bluish-grey, spongy nodules associated with scars over pressure points and easily traumatized areas like the elbows and knees.
Reference: HP:0000993
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandAbnormal perifollicular morphology (HP:0031285) help
..expandAnnular cutaneous lesion (HP:0025528) help
..expandAplasia/Hypoplasia of the skin (HP:0008065) help
..expandAtypical scarring of skin (HP:0000987) help
..expandCafe-au-lait spot (HP:0000957) help
..expandCapillary malformation (HP:0025104) help
..expandComedo (HP:0025249) help
..expandCutaneous cyst (HP:0025245) help
..expandHypopigmented skin patches (HP:0001053) help
..expandLichenoid skin lesion (HP:0031452) help
..expandMacule (HP:0012733) help
..expandMilia (HP:0001056) help
..expandNevus (HP:0003764) help
..expandPapule (HP:0200034) help
..expandSerpiginous cutaneous lesion (HP:0025527) help
..expandSkin dimple (HP:0010781) help
..expandSkin erosion (HP:0200041) help
..expandSkin fissure (HP:0031057) help
..expandSkin nodule (HP:0200036) help
..expandSkin pit (HP:0100276) help
..expandSkin plaque (HP:0200035) help
..expandSkin tags (HP:0010609) help
..expandSkin ulcer (HP:0200042) help
..expandSkin vesicle (HP:0200037) help
..expandXanthomatosis (HP:0000991) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0000993HP:0000993Molluscoid pseudotumors0COL1A1 CL E G H12772197ORPHA:287Classical Ehlers-Danlos syndromeHP:0040283 - Occasional373
HP:0000993HP:0000993Molluscoid pseudotumors0COL3A1 CL E G H12812201OMIM:130050Ehlers-Danlos syndrome, Vascular type.749
HP:0000993HP:0000993Molluscoid pseudotumors0COL5A1 CL E G H12892209ORPHA:287Classical Ehlers-Danlos syndromeHP:0040283 - Occasional660
HP:0000993HP:0000993Molluscoid pseudotumors0COL5A1 CL E G H12892209OMIM:130000Ehlers-danlos syndrome, type I660
HP:0000993HP:0000993Molluscoid pseudotumors0COL5A2 CL E G H12902210ORPHA:287Classical Ehlers-Danlos syndromeHP:0040283 - Occasional325
HP:0000993HP:0000993Molluscoid pseudotumors0COL5A2 CL E G H12902210OMIM:130010Ehlers-Danlos syndrome, classic type, 2325
HP:0000993HP:0000993Molluscoid pseudotumors0PLOD1 CL E G H53519081OMIM:225400Ehlers-Danlos syndrome, kyphoscoliotic type, 1.105
HP:0000993HP:0000993Molluscoid pseudotumors0ZNF469 CL E G H8462723216OMIM:229200Brittle cornea syndrome.397

Genes (6) :COL1A1 COL3A1 COL5A1 COL5A2 PLOD1 ZNF469

Diseases (6) :ORPHA:287 OMIM:130050 OMIM:130000 OMIM:130010 OMIM:225400 OMIM:229200

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.