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Cat (Felis catus) — Holoprosencephaly (hereditary; OMIA-verified species predisposition)

companion_species_health_holoprosencephaly_cat

companion-species-health 787 tok en 2026-08-24

Cat (Felis catus) — Holoprosencephaly (hereditary; OMIA-verified species predisposition)

Source: first-hand OMIA (University of Sydney) species-specific hereditary-disorder record, saved verbatim to source_file; every claim below is a C1 byte-substring of it.

Claims

  • Species: Cat (Felis catus)
  • Disorder: Holoprosencephaly
  • Summary: Information previously listed here relating to disease caused by variants in the GDF7 gene has been moved to:& OMIA:002366-9685 : Forebrain commissural malformation, ventriculomegaly and interhemispheric cysts, GDF7-related in Felis catus.

Evidence (references)

Derived from OMIA database dump (omia.xml, local); structured field, not verbatim prose. First-hand values below are verbatim substrings of the topic's pdf-raw/omia/<phene_id>.txt source file.

  • 2022. Successful treatment of hypodipsic/adipsic hypernatremia in a cat with lobar holoprosencephaly using oral desmopressin. JFMS Open Rep — PubMed:PMID35342639 | DOI:10.1177/20551169221082542 — OMIA Phene_Article / Article

Comparative medicine (human OMIM)

Derived from OMIA database dump (omia.xml, local); structured field, not verbatim prose. First-hand values below are verbatim substrings of the topic's pdf-raw/omia/<phene_id>.txt source file.

  • OMIM:236100 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:157170 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:142945 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:142946 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:609637 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:605934 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:610828 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:609408 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:610829 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:614226 (type: trait) — OMIA Group_OMIM (via OMIA_ID)

Evidence (references)

Derived from OMIA database dump (omia.xml, local); structured field, not verbatim prose. First-hand values below are verbatim substrings of the topic's pdf-raw/omia/<phene_id>.txt source file.

  • 2022. Successful treatment of hypodipsic/adipsic hypernatremia in a cat with lobar holoprosencephaly using oral desmopressin. JFMS Open Rep — PubMed:PMID35342639 | DOI:10.1177/20551169221082542 — OMIA Phene_Article / Article

Comparative medicine (human OMIM)

Derived from OMIA database dump (omia.xml, local); structured field, not verbatim prose. First-hand values below are verbatim substrings of the topic's pdf-raw/omia/<phene_id>.txt source file.

  • OMIM:236100 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:157170 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:142945 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:142946 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:609637 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:605934 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:610828 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:609408 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:610829 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:614226 (type: trait) — OMIA Group_OMIM (via OMIA_ID)

Sources

Cat (Felis catus) — Holoprosencephaly (hereditary; OMIA-verified species predisposition)
Source document: OMIA — Online Mendelian Inheritance in Animals (University of Sydney)
OMIA — Online Mendelian Inheritance in Animals (University of Sydney)OMIA species-specific hereditary-disorder records (omia.org), derived from local OMIA database dump; dataset: https://doi.org/10.25910/2AMR-PV70retrieved 2026-08-24

Verification file: pdf-raw/species-health/cat_holoprosencephaly_3826.txt

Machine access

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