From HPO
Small hand- MedGen UID:
- 108279
- •Concept ID:
- C0575802
- •
- Finding
Disproportionately small hand.
Absent distal phalanges- MedGen UID:
- 396111
- •Concept ID:
- C1861339
- •
- Finding
Aplasia (absence) of the distal phalanges.
2-5 finger cutaneous syndactyly- MedGen UID:
- 870711
- •Concept ID:
- C4025165
- •
- Anatomical Abnormality
A soft tissue continuity in the anteroposterior axis between the second to the fifth fingers that extends distally to at least the level of the proximal interphalangeal joints.
Low-set ears- MedGen UID:
- 65980
- •Concept ID:
- C0239234
- •
- Congenital Abnormality
Upper insertion of the ear to the scalp below an imaginary horizontal line drawn between the inner canthi of the eye and extending posteriorly to the ear.
Overfolded helix- MedGen UID:
- 325239
- •Concept ID:
- C1837731
- •
- Finding
A condition in which the helix is folded over to a greater degree than normal. That is, excessive curling of the helix edge, whereby the free edge is parallel to the plane of the ear.
Micrognathia- MedGen UID:
- 44428
- •Concept ID:
- C0025990
- •
- Congenital Abnormality
Developmental hypoplasia of the mandible.
Prominent occiput- MedGen UID:
- 381255
- •Concept ID:
- C1853737
- •
- Finding
Increased convexity of the occiput (posterior part of the skull).
Wide anterior fontanel- MedGen UID:
- 400926
- •Concept ID:
- C1866134
- •
- Finding
Enlargement of the anterior fontanelle with respect to age-dependent norms.
Ankyloblepharon- MedGen UID:
- 83282
- •Concept ID:
- C0339182
- •
- Anatomical Abnormality
Partial fusion of the upper and lower eyelid margins by single or multiple bands of tissue.
Bilateral cleft lip- MedGen UID:
- 451046
- •Concept ID:
- C0392005
- •
- Congenital Abnormality
A non-midline cleft of the upper lip on the left and right sides.
Bilateral cleft palate- MedGen UID:
- 765998
- •Concept ID:
- C3553084
- •
- Finding
Nonmidline cleft palate on the left and right sides.
Accessory oral frenulum- MedGen UID:
- 867439
- •Concept ID:
- C4021814
- •
- Congenital Abnormality
Extra fold of tissue extending from the alveolar ridge to the inner surface of the upper or lower lip.
Axillary pterygium- MedGen UID:
- 335019
- •Concept ID:
- C1844738
- •
- Finding
Presence of a cutaneous membrane (flap) in the armpit.
Antecubital pterygium syndrome- MedGen UID:
- 401231
- •Concept ID:
- C1867439
- •
- Disease or Syndrome
Antecubital pterygium syndrome is an autosomal dominant disorder characterized by a fleshy web extending across the anterior aspect of the cubital fossa, absence of the long head of the triceps, limitation of full elbow extension, and missing skin creases over the terminal interphalangeal joints of the fingers (summary by Wallis et al., 1988).
Popliteal pterygium- MedGen UID:
- 811750
- •Concept ID:
- C3805420
- •
- Finding
A pterygium (or pterygia) occurring in the popliteal region (the back of the knee).
Corneal opacity- MedGen UID:
- 40485
- •Concept ID:
- C0010038
- •
- Finding
A reduction of corneal clarity.
Microphthalmia- MedGen UID:
- 10033
- •Concept ID:
- C0026010
- •
- Congenital Abnormality
Microphthalmia is an eye abnormality that arises before birth. In this condition, one or both eyeballs are abnormally small. In some affected individuals, the eyeball may appear to be completely missing; however, even in these cases some remaining eye tissue is generally present. Such severe microphthalmia should be distinguished from another condition called anophthalmia, in which no eyeball forms at all. However, the terms anophthalmia and severe microphthalmia are often used interchangeably. Microphthalmia may or may not result in significant vision loss.\n\nPeople with microphthalmia may also have a condition called coloboma. Colobomas are missing pieces of tissue in structures that form the eye. They may appear as notches or gaps in the colored part of the eye called the iris; the retina, which is the specialized light-sensitive tissue that lines the back of the eye; the blood vessel layer under the retina called the choroid; or in the optic nerves, which carry information from the eyes to the brain. Colobomas may be present in one or both eyes and, depending on their size and location, can affect a person's vision.\n\nPeople with microphthalmia may also have other eye abnormalities, including clouding of the lens of the eye (cataract) and a narrowed opening of the eye (narrowed palpebral fissure). Additionally, affected individuals may have an abnormality called microcornea, in which the clear front covering of the eye (cornea) is small and abnormally curved.\n\nBetween one-third and one-half of affected individuals have microphthalmia as part of a syndrome that affects other organs and tissues in the body. These forms of the condition are described as syndromic. When microphthalmia occurs by itself, it is described as nonsyndromic or isolated.
- Abnormality of head or neck
- Abnormality of limbs
- Abnormality of the eye
- Abnormality of the integument
- Abnormality of the musculoskeletal system
- Ear malformation