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cryptophthalmos

congenital abnormality characterized by the presence of a continuous layer of skin extending over the eyeballs and the absence of eyelids and the palpebral fissure
Class type of: eyelid disease, congenital disorder Q590324

Facts

7 properties
Instance of
class of disease
Subclass of
eyelid disease, congenital disorder
Genetic association
GRIP1, FRAS1, FREM2[7][8][9]
Health specialty
medical genetics[6]
ICD-9-CM
743.06[4]
NCI Thesaurus ID
C124520[5]
P14914
D98562[10]
🏷️ Also known as
en cryptophthalmos en Cryptophthalmia el κρυπτοφθαλμία el κρυπτόφθαλμος fr cryptophtalmie pl Skrytoocze ru Криптофтальм
🔖 Identifiers · 14
Disease Ontology ID
DOID:0111716
DiseasesDB
29617
Exact match
www.orpha.net, purl.obolibrary.org, identifiers.org
GARD rare disease ID
10505
Human Phenotype Ontology ID
HP:0001126
ICD-10 ID
Q11.2
ICD-11 ID (Foundation)
740223582
ICD-11 ID (MMS)
LA14.01
ICD-9 ID
743.06
Medical Dictionary for Regulatory Activities ID
10027548
Microsoft Academic ID (discontinued)
2777387926
Mondo ID
MONDO_0020153
Show all 14 identifiers +2
Orphanet ID
98562
UMLS CUI
C0311249

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Summary

cryptophthalmos is a class of disease[1]. cryptophthalmos is a type of eyelid disease[2] and congenital disorder[3].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . Disease Ontology. Retrieved . wikidata.org.
  3. [4] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  4. [5] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . Retrieved . wikidata.org.
  7. [8] ↑ . Retrieved . wikidata.org.
  8. [9] ↑ . Retrieved . wikidata.org.
  9. [10] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). cryptophthalmos. Retrieved November 4, 2026, from https://4ort.xyz/entity/cryptophthalmos
MLA “cryptophthalmos.” 4ort.xyz Knowledge Graph, 4ort.xyz, 4 Nov. 2026, https://4ort.xyz/entity/cryptophthalmos.
BibTeX @misc{4ortxyz_cryptophthalmos_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{cryptophthalmos}}, year = {2026}, url = {https://4ort.xyz/entity/cryptophthalmos}, note = {Accessed: 2026-11-04}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): cryptophthalmos — https://4ort.xyz/entity/cryptophthalmos (retrieved 2026-11-04)

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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 12d ago · ACorrêa (WMB) · 2026-10-24 view diff on Wikidata ↗
    Genetic association → GRIP1, FRAS1, FREM2
    P14914 → D98562
    Claims rich → —
    "/* wbeditentity-update-languages-and-other-short:0||pt, pt-br */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/61469|batch #61469]]: Raras.org data import"
  2. 4w ago · عُثمان · 2026-10-04 view diff on Wikidata ↗
    Disease Ontology ID → DOID:0111716
    Sitelink count → 4
    ICD-11 ID (MMS) → LA14.01
    Microsoft Academic ID (discontinued) → 2777387926
    + 20 other properties edited (see Wikidata diff for full list)
    "/* wbsetclaim-create:1||1 */ Human Phenotype Ontology ID: HP:0001126, Matched to [[:toollabs:mix-n-match/#/entry/19251402|Cryptophthalmos (#19251402)]] in [[:toollabs:mix-n-match/#/catalog/405|HPO]] #"
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